Transcription-terminating mutation in telethonin causing...

Neuromuscular Disorders 2008 Vol. 18; Iss. 12

Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient

Montse Olivé, Alexey Shatunov, Laura Gonzalez, Olga Carmona, Dolores Moreno, Lidia Gonzalez Quereda, J.A. Martinez-Matos, Lev G. Goldfarb, Isidro Ferrer
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Volume:
18
Year:
2008
Language:
english
DOI:
10.1016/j.nmd.2008.07.009
File:
PDF, 477 KB
english, 2008
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