about
Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication.Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.Charcot-Marie-Tooth disease type 1Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families.Phenotypic heterogeneity and the single gene.What's the Function of Connexin 32 in the Peripheral Nervous System?
P2860
description
1991 nî lūn-bûn
@nan
1991 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Hereditary motor and sensory neuropathies.
@ast
Hereditary motor and sensory neuropathies.
@en
type
label
Hereditary motor and sensory neuropathies.
@ast
Hereditary motor and sensory neuropathies.
@en
prefLabel
Hereditary motor and sensory neuropathies.
@ast
Hereditary motor and sensory neuropathies.
@en
P2860
P356
P1476
Hereditary motor and sensory neuropathies.
@en
P2093
P2860
P356
10.1136/JMG.28.1.1
P407
P577
1991-01-01T00:00:00Z