about
The puzzle of TRPV4 channelopathies.Connexinopathies: a structural and functional glimpseMolecular genetics of charcot-marie-tooth disease: from genes to genomes.Functional requirement for a highly conserved charged residue at position 75 in the gap junction protein connexin 32.Murine therapeutic models for Charcot-Marie-Tooth (CMT) disease.Proptosis in a family with the p16 Leuc-to-Prol mutation in the PMP22 gene (CMT 1E).Neurogenetics in Argentina: diagnostic yield in a personalized research based clinic.Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth disease.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
Genetics of neuropathies.
@en
Genetics of neuropathies.
@nl
type
label
Genetics of neuropathies.
@en
Genetics of neuropathies.
@nl
prefLabel
Genetics of neuropathies.
@en
Genetics of neuropathies.
@nl
P356
P1476
Genetics of neuropathies.
@en
P2093
Carly E Siskind
Michael E Shy
P304
P356
10.1055/S-0031-1299788
P577
2011-11-01T00:00:00Z