N.P.3 02 Wide clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2 gene

✍ Scribed by J. Colomer; R. Gooding; D. Angelicheva; R.H.M. King; Y. Parman; A. Nascimento; J. Conill; L. Kalaydjieva

• Book ID: 116792535
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 57 KB
• Volume: 16
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2006.05.078