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

Published 2008 View Full Article

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Title
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 17, Issue 24, Pages 4022-4035
Publisher
Oxford University Press (OUP)
Online
2008-09-21
DOI
10.1093/hmg/ddn305
References
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