N.P.3 02 Wide clinical spectrum of CMT4C disease in...

Neuromuscular Disorders 2006 Vol. 16; Iss. 9-10

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

J. Colomer, R. Gooding, D. Angelicheva, R.H.M. King, Y. Parman, A. Nascimento, J. Conill, L. Kalaydjieva
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Volume:
16
Year:
2006
Language:
english
DOI:
10.1016/j.nmd.2006.05.078
File:
PDF, 57 KB
english, 2006
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