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

Akio Masuda, Xin Ming Shen, Mikako Ito, Tohru Matsuura, Andrew G. Engel, Kinji Ohno

Research output: Contribution to journal › Article › peer-review

38 Scopus citations

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Medicine & Life Sciences