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

Saved in:
Bibliographic Details
Published in:Neuromuscular disorders : NMD 2006-10, Vol.16 (9), p.664-665
Main Authors: Colomer, J., Gooding, R., Angelicheva, D., King, R.H.M., Parman, Y., Nascimento, A., Conill, J., Kalaydjieva, L.
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:0960-8966
1873-2364
DOI:10.1016/j.nmd.2006.05.078