Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama
Several members of a large Caucasian family who presented with a congenital Heinz body hemolytic anemia were found to be carriers of the unstable Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2. Identification by protein analysis was hampered by the instability of the variant which complicated its i...
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| Veröffentlicht in: | Hemoglobin 1995-05, Vol.19 (3-4), p.151-164 |
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| container_title | Hemoglobin |
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| creator | Prchal, J T Adler, B Wilson, J B Baysal, E Qin, W B Molchanova, T P Pobedimskaya, D D Kazanetz, E G Huisman, T H |
| description | Several members of a large Caucasian family who presented with a congenital Heinz body hemolytic anemia were found to be carriers of the unstable Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2. Identification by protein analysis was hampered by the instability of the variant which complicated its isolation from shipped blood samples. Moreover, the detection of the CTG-->CCG mutation at codon 136 of the alpha 2 gene required the substitution of dGTP by dITP during the DNA sequencing process to prevent the occurrence of secondary structures and compressions in the sequencing gel. The first Hb Bibba heterozygote, characterized in 1968 (1), is believed to be a member of this family. The clinical expression of the disease is surprisingly variable. |
| doi_str_mv | 10.3109/03630269509036935 |
| format | Article |
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Identification by protein analysis was hampered by the instability of the variant which complicated its isolation from shipped blood samples. Moreover, the detection of the CTG-->CCG mutation at codon 136 of the alpha 2 gene required the substitution of dGTP by dITP during the DNA sequencing process to prevent the occurrence of secondary structures and compressions in the sequencing gel. The first Hb Bibba heterozygote, characterized in 1968 (1), is believed to be a member of this family. The clinical expression of the disease is surprisingly variable.</description><identifier>ISSN: 0363-0269</identifier><identifier>EISSN: 1532-432X</identifier><identifier>DOI: 10.3109/03630269509036935</identifier><identifier>PMID: 7558871</identifier><language>eng</language><publisher>England</publisher><subject>Alabama ; Amino Acid Sequence ; Anemia, Hemolytic, Congenital - blood ; Anemia, Hemolytic, Congenital - genetics ; Base Sequence ; DNA Mutational Analysis ; Electrophoresis, Polyacrylamide Gel ; European Continental Ancestry Group - genetics ; Female ; Genetic Variation ; Globins - genetics ; Heinz Bodies - ultrastructure ; Hemoglobins, Abnormal - chemistry ; Hemoglobins, Abnormal - genetics ; Heterozygote ; Humans ; Male ; Molecular Sequence Data ; Pedigree ; Point Mutation</subject><ispartof>Hemoglobin, 1995-05, Vol.19 (3-4), p.151-164</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1431-8d488ec2392768d3a1e401eade26677468ed12beb97ec5ec6087b2a767f115873</citedby><cites>FETCH-LOGICAL-c1431-8d488ec2392768d3a1e401eade26677468ed12beb97ec5ec6087b2a767f115873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7558871$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Prchal, J T</creatorcontrib><creatorcontrib>Adler, B</creatorcontrib><creatorcontrib>Wilson, J B</creatorcontrib><creatorcontrib>Baysal, E</creatorcontrib><creatorcontrib>Qin, W B</creatorcontrib><creatorcontrib>Molchanova, T P</creatorcontrib><creatorcontrib>Pobedimskaya, D D</creatorcontrib><creatorcontrib>Kazanetz, E G</creatorcontrib><creatorcontrib>Huisman, T H</creatorcontrib><title>Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama</title><title>Hemoglobin</title><addtitle>Hemoglobin</addtitle><description>Several members of a large Caucasian family who presented with a congenital Heinz body hemolytic anemia were found to be carriers of the unstable Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2. Identification by protein analysis was hampered by the instability of the variant which complicated its isolation from shipped blood samples. Moreover, the detection of the CTG-->CCG mutation at codon 136 of the alpha 2 gene required the substitution of dGTP by dITP during the DNA sequencing process to prevent the occurrence of secondary structures and compressions in the sequencing gel. The first Hb Bibba heterozygote, characterized in 1968 (1), is believed to be a member of this family. The clinical expression of the disease is surprisingly variable.</description><subject>Alabama</subject><subject>Amino Acid Sequence</subject><subject>Anemia, Hemolytic, Congenital - blood</subject><subject>Anemia, Hemolytic, Congenital - genetics</subject><subject>Base Sequence</subject><subject>DNA Mutational Analysis</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>European Continental Ancestry Group - genetics</subject><subject>Female</subject><subject>Genetic Variation</subject><subject>Globins - genetics</subject><subject>Heinz Bodies - ultrastructure</subject><subject>Hemoglobins, Abnormal - chemistry</subject><subject>Hemoglobins, Abnormal - genetics</subject><subject>Heterozygote</subject><subject>Humans</subject><subject>Male</subject><subject>Molecular Sequence Data</subject><subject>Pedigree</subject><subject>Point Mutation</subject><issn>0363-0269</issn><issn>1532-432X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplkE9Lw0AQxRdRaq1-AA_CnkQP0Z3dZP9chFrUCoV6UPAWZpMJRpKm7jaHfntTWrx4mgfv9x7MY-wSxJ0C4e6F0kpI7TLhBulUdsTGkCmZpEp-HrPxzk92wCk7i_FbCHBGpCM2MllmrYExW849f6y9R94Fjs36C7nkoPTNHNztgvokeXgLHfe02Rn1iiOfYV9grHHFK2zrZsur0LV82qDHFs_ZSYVNpIvDnbCP56f32TxZLF9eZ9NFUkCqILFlai0VUjlptC0VAqUCCEuSWhuTakslSE_eGSoyKrSwxks02lQAmTVqwq73vevQ_fQUN3lbx4KaBlfU9TE3ZqCGzwcQ9mARuhgDVfk61C2GbQ4i342Y_xtxyFwdynvfUvmXOKymfgHS2Gdm</recordid><startdate>199505</startdate><enddate>199505</enddate><creator>Prchal, J T</creator><creator>Adler, B</creator><creator>Wilson, J B</creator><creator>Baysal, E</creator><creator>Qin, W B</creator><creator>Molchanova, T P</creator><creator>Pobedimskaya, D D</creator><creator>Kazanetz, E G</creator><creator>Huisman, T H</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199505</creationdate><title>Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama</title><author>Prchal, J T ; Adler, B ; Wilson, J B ; Baysal, E ; Qin, W B ; Molchanova, T P ; Pobedimskaya, D D ; Kazanetz, E G ; Huisman, T H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1431-8d488ec2392768d3a1e401eade26677468ed12beb97ec5ec6087b2a767f115873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Alabama</topic><topic>Amino Acid Sequence</topic><topic>Anemia, Hemolytic, Congenital - blood</topic><topic>Anemia, Hemolytic, Congenital - genetics</topic><topic>Base Sequence</topic><topic>DNA Mutational Analysis</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>European Continental Ancestry Group - genetics</topic><topic>Female</topic><topic>Genetic Variation</topic><topic>Globins - genetics</topic><topic>Heinz Bodies - ultrastructure</topic><topic>Hemoglobins, Abnormal - chemistry</topic><topic>Hemoglobins, Abnormal - genetics</topic><topic>Heterozygote</topic><topic>Humans</topic><topic>Male</topic><topic>Molecular Sequence Data</topic><topic>Pedigree</topic><topic>Point Mutation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prchal, J T</creatorcontrib><creatorcontrib>Adler, B</creatorcontrib><creatorcontrib>Wilson, J B</creatorcontrib><creatorcontrib>Baysal, E</creatorcontrib><creatorcontrib>Qin, W B</creatorcontrib><creatorcontrib>Molchanova, T P</creatorcontrib><creatorcontrib>Pobedimskaya, D D</creatorcontrib><creatorcontrib>Kazanetz, E G</creatorcontrib><creatorcontrib>Huisman, T H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Hemoglobin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prchal, J T</au><au>Adler, B</au><au>Wilson, J B</au><au>Baysal, E</au><au>Qin, W B</au><au>Molchanova, T P</au><au>Pobedimskaya, D D</au><au>Kazanetz, E G</au><au>Huisman, T H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama</atitle><jtitle>Hemoglobin</jtitle><addtitle>Hemoglobin</addtitle><date>1995-05</date><risdate>1995</risdate><volume>19</volume><issue>3-4</issue><spage>151</spage><epage>164</epage><pages>151-164</pages><issn>0363-0269</issn><eissn>1532-432X</eissn><abstract>Several members of a large Caucasian family who presented with a congenital Heinz body hemolytic anemia were found to be carriers of the unstable Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2. Identification by protein analysis was hampered by the instability of the variant which complicated its isolation from shipped blood samples. Moreover, the detection of the CTG-->CCG mutation at codon 136 of the alpha 2 gene required the substitution of dGTP by dITP during the DNA sequencing process to prevent the occurrence of secondary structures and compressions in the sequencing gel. The first Hb Bibba heterozygote, characterized in 1968 (1), is believed to be a member of this family. The clinical expression of the disease is surprisingly variable.</abstract><cop>England</cop><pmid>7558871</pmid><doi>10.3109/03630269509036935</doi><tpages>14</tpages></addata></record> |
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| identifier | ISSN: 0363-0269 |
| ispartof | Hemoglobin, 1995-05, Vol.19 (3-4), p.151-164 |
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| language | eng |
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| source | Taylor & Francis; MEDLINE; Taylor & Francis Medical Library - CRKN |
| subjects | Alabama Amino Acid Sequence Anemia, Hemolytic, Congenital - blood Anemia, Hemolytic, Congenital - genetics Base Sequence DNA Mutational Analysis Electrophoresis, Polyacrylamide Gel European Continental Ancestry Group - genetics Female Genetic Variation Globins - genetics Heinz Bodies - ultrastructure Hemoglobins, Abnormal - chemistry Hemoglobins, Abnormal - genetics Heterozygote Humans Male Molecular Sequence Data Pedigree Point Mutation |
| title | Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama |
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