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

Author: Masuda Akio   Shen Xin-Ming   Ito Mikako   Matsuura Tohru   Engel Andrew G.   Ohno Kinji  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.17, Iss.24, 2008-12, pp. : 4022-4035

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