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

Source:http://linkedlifedata.com/resource/pubmed/id/18806275

Hum. Mol. Genet. 2008 Dec 15 17 24 4022-35

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PMID
18806275