G.P.121 X-linked recessive distal myopathy with hypertrophic cardiomyopathy caused by a novel mutation in the FHL1 gene

✍ Scribed by D’Arcy, C.E.; Kanellakis, V.; Ryan, M.M.; McLean, C.A.

• Book ID: 119333953
• Publisher: Elsevier Science
• Year: 2012
• Tongue: English
• Weight: 61 KB
• Volume: 22
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2012.06.327