P.1.12 Whole exome sequencing as a genetic diagnostic tool...

Neuromuscular Disorders 2013 / 10 Vol. 23; Iss. 9-10

P.1.12 Whole exome sequencing as a genetic diagnostic tool for congenital muscular dystrophies

Ceyhan, O., Talim, B., Beggs, A.H., Topaloglu, H.
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Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.396
Date:
October, 2013
File:
PDF, 44 KB
english, 2013
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