G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu↑Lys mutation

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Bibliographische Detailangaben
Veröffentlicht in:	Human molecular genetics 1992-06, Vol.1 (3), p.209-210
Hauptverfasser:	Ahluwalia, A., Corcoran, C.M., Vulliamy, T.J., Ishwad, C.S., Naidu, J.M., Argusti, A., Stevens, D.J., Mason, P.J., Luzzatto, L.
Format:	Artikel
Sprache:	eng
Schlagworte:	Amino Acid Sequence Anemias. Hemoglobinopathies Base Sequence Biological and medical sciences Cloning, Molecular Diseases of red blood cells DNA - genetics Genetic Variation Glucosephosphate Dehydrogenase - genetics Glucosephosphate Dehydrogenase Deficiency - genetics Hematologic and hematopoietic diseases Humans India Medical sciences Molecular Sequence Data Point Mutation
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