Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis
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| Veröffentlicht in: | Brain (London, England : 1878) England : 1878), 2014-12, Vol.137 (Pt 12), p.e312-e312 |
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| container_issue | Pt 12 |
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| container_title | Brain (London, England : 1878) |
| container_volume | 137 |
| creator | Bannwarth, Sylvie Ait-El-Mkadem, Samira Chaussenot, Annabelle Genin, Emmanuelle C Lacas-Gervais, Sandra Fragaki, Konstantina Berg-Alonso, Laetitia Kageyama, Yusuke Serre, Valérie Moore, David Verschueren, Annie Rouzier, Cécile Le Ber, Isabelle Augé, Gaëlle Cochaud, Charlotte Lespinasse, Françoise N'Guyen, Karine de Septenville, Anne Brice, Alexis Yu-Wai-Man, Patrick Sesaki, Hiromi Pouget, Jean Paquis-Flucklinger, Véronique |
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| doi_str_mv | 10.1093/brain/awu267 |
| format | Article |
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Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-b73a73dea7f971827b02736134ebb70bc8bb827c578862b2a4fe02796392622f3</citedby><cites>FETCH-LOGICAL-c418t-b73a73dea7f971827b02736134ebb70bc8bb827c578862b2a4fe02796392622f3</cites><orcidid>0000-0002-0941-3990 ; 0000-0003-4117-2813 ; 0000-0003-1266-9062 ; 0000-0001-7847-9320</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25261971$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02108988$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Bannwarth, Sylvie</creatorcontrib><creatorcontrib>Ait-El-Mkadem, Samira</creatorcontrib><creatorcontrib>Chaussenot, Annabelle</creatorcontrib><creatorcontrib>Genin, Emmanuelle C</creatorcontrib><creatorcontrib>Lacas-Gervais, Sandra</creatorcontrib><creatorcontrib>Fragaki, Konstantina</creatorcontrib><creatorcontrib>Berg-Alonso, Laetitia</creatorcontrib><creatorcontrib>Kageyama, Yusuke</creatorcontrib><creatorcontrib>Serre, Valérie</creatorcontrib><creatorcontrib>Moore, David</creatorcontrib><creatorcontrib>Verschueren, Annie</creatorcontrib><creatorcontrib>Rouzier, Cécile</creatorcontrib><creatorcontrib>Le Ber, Isabelle</creatorcontrib><creatorcontrib>Augé, Gaëlle</creatorcontrib><creatorcontrib>Cochaud, Charlotte</creatorcontrib><creatorcontrib>Lespinasse, Françoise</creatorcontrib><creatorcontrib>N'Guyen, Karine</creatorcontrib><creatorcontrib>de Septenville, Anne</creatorcontrib><creatorcontrib>Brice, Alexis</creatorcontrib><creatorcontrib>Yu-Wai-Man, Patrick</creatorcontrib><creatorcontrib>Sesaki, Hiromi</creatorcontrib><creatorcontrib>Pouget, Jean</creatorcontrib><creatorcontrib>Paquis-Flucklinger, Véronique</creatorcontrib><title>Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis</title><title>Brain (London, England : 1878)</title><addtitle>Brain</addtitle><subject>Amyotrophic Lateral Sclerosis - etiology</subject><subject>DNA, Mitochondrial - genetics</subject><subject>Female</subject><subject>Frontotemporal Dementia - etiology</subject><subject>Humans</subject><subject>Letters to the Editor</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Mitochondria - pathology</subject><subject>Mitochondrial Diseases - complications</subject><subject>Mitochondrial Proteins - genetics</subject><issn>0006-8950</issn><issn>1460-2156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc2LFDEQxYMo7uzqzbPkqLDtVpLufHgQlvFjhBFB9Bwq2fROpLszJt0r89-bddZFPYSCl19eVeoR8ozBKwZGXLiMcbrAnwuX6gFZsVZCw1knH5IVAMhGmw5OyGkp3wFYK7h8TE54xyUziq0Ifgn74fCaflpmnGOaCo0TnXeBrjfrzVsG9DpMgWKuh_o0jmmiHpcSaOppj2McIg4Ux0Oac9rvoqcDziFXrfgh5FRieUIe9TiU8PSunpFv7999XW-a7ecPH9eX28a3TM-NUwKVuAqo-jqY5soBV0Iy0QbnFDivnauq75TWkjuObR8qYaQwXHLeizPy5ui7X9wYrnyY5jqH3ec4Yj7YhNH-ezPFnb1ON7bVYIzqqsHLo8Huv2eby6291YAz0EbrG1bZF3fNcvqxhDLbMRYfhgGnkJZimeQKlFDGVPT8iPq6jpJDf-_NwN4maH8naI8JVvz539-4h_9EJn4BLiuYMw</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Bannwarth, Sylvie</creator><creator>Ait-El-Mkadem, Samira</creator><creator>Chaussenot, Annabelle</creator><creator>Genin, Emmanuelle C</creator><creator>Lacas-Gervais, Sandra</creator><creator>Fragaki, Konstantina</creator><creator>Berg-Alonso, Laetitia</creator><creator>Kageyama, Yusuke</creator><creator>Serre, Valérie</creator><creator>Moore, David</creator><creator>Verschueren, Annie</creator><creator>Rouzier, Cécile</creator><creator>Le Ber, Isabelle</creator><creator>Augé, Gaëlle</creator><creator>Cochaud, Charlotte</creator><creator>Lespinasse, Françoise</creator><creator>N'Guyen, Karine</creator><creator>de Septenville, Anne</creator><creator>Brice, Alexis</creator><creator>Yu-Wai-Man, Patrick</creator><creator>Sesaki, Hiromi</creator><creator>Pouget, Jean</creator><creator>Paquis-Flucklinger, Véronique</creator><general>Oxford University Press</general><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><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0941-3990</orcidid><orcidid>https://orcid.org/0000-0003-4117-2813</orcidid><orcidid>https://orcid.org/0000-0003-1266-9062</orcidid><orcidid>https://orcid.org/0000-0001-7847-9320</orcidid></search><sort><creationdate>20141201</creationdate><title>Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis</title><author>Bannwarth, Sylvie ; Ait-El-Mkadem, Samira ; Chaussenot, Annabelle ; Genin, Emmanuelle C ; Lacas-Gervais, Sandra ; Fragaki, Konstantina ; Berg-Alonso, Laetitia ; Kageyama, Yusuke ; Serre, Valérie ; Moore, David ; Verschueren, Annie ; Rouzier, Cécile ; Le Ber, Isabelle ; Augé, Gaëlle ; Cochaud, Charlotte ; Lespinasse, Françoise ; N'Guyen, Karine ; de Septenville, Anne ; Brice, Alexis ; Yu-Wai-Man, Patrick ; Sesaki, Hiromi ; Pouget, Jean ; Paquis-Flucklinger, Véronique</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-b73a73dea7f971827b02736134ebb70bc8bb827c578862b2a4fe02796392622f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Amyotrophic Lateral Sclerosis - 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| fulltext | fulltext |
| identifier | ISSN: 0006-8950 |
| ispartof | Brain (London, England : 1878), 2014-12, Vol.137 (Pt 12), p.e312-e312 |
| issn | 0006-8950 1460-2156 |
| language | eng |
| recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4809975 |
| source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
| subjects | Amyotrophic Lateral Sclerosis - etiology DNA, Mitochondrial - genetics Female Frontotemporal Dementia - etiology Humans Letters to the Editor Life Sciences Male Mitochondria - pathology Mitochondrial Diseases - complications Mitochondrial Proteins - genetics |
| title | Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis |
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