about
De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)Dejerine-Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients.Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation.Hereditary demyelinating motor and sensory neuropathy.Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood.
P2860
description
1984 nî lūn-bûn
@nan
1984 թուականին հրատարակուած գիտական յօդուած
@hyw
1984 թվականին հրատարակված գիտական հոդված
@hy
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
name
Two cases of congenital hypomyelination neuropathy
@ast
Two cases of congenital hypomyelination neuropathy
@en
Two cases of congenital hypomyelination neuropathy
@nl
type
label
Two cases of congenital hypomyelination neuropathy
@ast
Two cases of congenital hypomyelination neuropathy
@en
Two cases of congenital hypomyelination neuropathy
@nl
prefLabel
Two cases of congenital hypomyelination neuropathy
@ast
Two cases of congenital hypomyelination neuropathy
@en
Two cases of congenital hypomyelination neuropathy
@nl
P2093
P1476
Two cases of congenital hypomyelination neuropathy
@en
P2093
P356
10.1016/S0387-7604(84)80101-1
P407
P577
1984-01-01T00:00:00Z