Myotonia congenita in a large consanguineous arab family: insight into the clinical spectrum of carriers and double heterozygotes of a novel mutation in the chloride channel clcn1 gene. A – The Adir Lab

Myotonia congenita in a large consanguineous arab family: insight into the clinical spectrum of carriers and double heterozygotes of a novel mutation in the chloride channel clcn1 gene. A

Authors:

A. Shalata, H. Furman, V. Adir, N. Adir, Y. Hujeirat, S. A. Shalev and Zvi U. Borochowitz

Muscle and Nerve 41, 464-9 (2010)

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