Novel MPZ mutations and congenital hypomyelinating neuropathy
about
Demyelinating prenatal and infantile developmental neuropathies.Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy.Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy.Congenital hypomyelinating neuropathy due to a novel MPZ mutation
P2860
Novel MPZ mutations and congenital hypomyelinating neuropathy
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Novel MPZ mutations and congenital hypomyelinating neuropathy
@en
type
label
Novel MPZ mutations and congenital hypomyelinating neuropathy
@en
prefLabel
Novel MPZ mutations and congenital hypomyelinating neuropathy
@en
P2093
P2860
P1476
Novel MPZ mutations and congenital hypomyelinating neuropathy
@en
P2093
Frederic Shapiro
Libby Couchon
Peter B Kang
Sandro Santagata
Sat Dev Batish
Stephen Donnelly
P2860
P304
P356
10.1016/J.NMD.2010.06.004
P577
2010-11-01T00:00:00Z