A candidate gene for autoimmune myasthenia gravis

OBJECTIVE: We sought to identify a causative mutation in a previously reported kindred with parental consanguinity and 5 of 10 siblings with adult-onset autoimmune myasthenia gravis. METHODS: We performed genome-wide homozygosity mapping, and sequenced all known genes in the one region of extended h...

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Main Authors: Landouré, Guida, Knight, Melanie A., Stanescu, Horia, Taye, Addis A., Shi, Yijun, Diallo, Oumarou, Johnson, Janel O., Hernandez, Dena, Traynor, Bryan J., Biesecker, Leslie G., Elkahloun, Abdel, Rinaldi, Carlo, Vincent, Angela, Willcox, Nick, Kleta, Robert, Fischbeck, Kenneth H., Burnett, Barrington G.
Formáid: Artigo
Teanga:Inglês
Foilsithe: Lippincott Williams & Wilkins 2012
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Articles
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3400092/
https://ncbi.nlm.nih.gov/pubmed/22744667
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e318260cbd0
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