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Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene

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Bibliographic Details
Main Author:	Fernando Morales
Format:	Artículo científico
Language:	en
Published:	Universidad de Costa Rica 2008
Subjects:	Biología SSCP Becker myotonia Myotonia congenita myotonic dystrophy chloride channelopathy
Online Access:	Acceder al recurso
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