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A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase loci
Norma Beatriz Romero, Dominique Récan, Odile Rigal, France Leturcq, Stéphane Llense, Jean-Claude Barbot, Nathalie Deburgrave, Marie Armelle Cheval, Françoise Deniau, Jean-Claude KaplanVolume:
7
Year:
1997
Language:
english
DOI:
10.1016/s0960-8966(97)00114-4
File:
PDF, 308 KB
english, 1997