hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome

出版年份 2008 全文链接

标题

作者

关键词

出版物

Volume 17, Issue 24, Pages 4022-4035

出版商

Oxford University Press (OUP)

发表日期

2008-09-21

DOI

10.1093/hmg/ddn305

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