Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.
about
Tracing myelin protein zero (P0) in vivo by construction of P0-GFP fusion proteinsA second locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 19q13.3.Neuropathology of Charcot-Marie-Tooth and related disorders.Homozygous inactivation of the LGI1 gene results in hypomyelination in the peripheral and central nervous systems.The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy.Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models
P2860
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.
description
1999 nî lūn-bûn
@nan
1999 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.
@ast
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.
@en
type
label
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.
@ast
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.
@en
prefLabel
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.
@ast
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.
@en
P2093
P356
P1433
P1476
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.
@en
P2093
De Jonghe P
Rautenstrauss B
Timmerman V
Van Broeckhoven C
P2888
P304
P356
10.1007/S100480050074
P577
1999-09-01T00:00:00Z