about
Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndrome.The homozygous ganglioside-induced differentiation-associated protein 1 mutation c.373C > T causes a very early-onset neuropathy: case report and literature review.Mutations in the LMNA gene do not cause axonal CMT in Czech patients.Molecular analysis of the genes causing recessive demyelinating Charcot-Marie-Tooth disease in Japan.
P2860
description
2007 nî lūn-bûn
@nan
2007 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
GDAP1 mutations in Czech families with early-onset CMT
@ast
GDAP1 mutations in Czech families with early-onset CMT
@en
GDAP1 mutations in Czech families with early-onset CMT
@nl
type
label
GDAP1 mutations in Czech families with early-onset CMT
@ast
GDAP1 mutations in Czech families with early-onset CMT
@en
GDAP1 mutations in Czech families with early-onset CMT
@nl
prefLabel
GDAP1 mutations in Czech families with early-onset CMT
@ast
GDAP1 mutations in Czech families with early-onset CMT
@en
GDAP1 mutations in Czech families with early-onset CMT
@nl
P2093
P1476
GDAP1 mutations in Czech families with early-onset CMT
@en
P2093
Baránková L
De Jonghe P
Sakmaryová I
Vondrácek P
Vyhnálková E
P304
P356
10.1016/J.NMD.2007.02.010
P407
P577
2007-04-11T00:00:00Z