Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

Author： Muchir Antoine   Bonne Gisèle   van der Kooi Anneke J.   van Mia   Baas Frank   Bolhuis Pieter A.   de Marianne   Schwartz Ketty  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.9, Iss.9, 2000-05, pp. : 1453-1459

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