Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1
about
The genetics of Charcot-Marie-Tooth disease: current trends and future implications for diagnosis and managementGenotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.Connexins in hearing loss: a comprehensive overview.Charcot-marie-tooth disease: seventeen causative genes.
P2860
Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1
description
article
@en
im Jahr 2003 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 2002
@uk
name
Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1
@en
Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1
@nl
type
label
Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1
@en
Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1
@nl
prefLabel
Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1
@en
Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1
@nl
P2093
P50
P356
P1433
P1476
Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1
@en
P2093
Bernd W Rautenstrauss
Christoph J Ploner
Cornelia Kraus
Hans Dieter Rott
Johannes Kotzian
Kathrin Huehne
Vladimir Benes
Wolfram Kress
P356
10.1002/HUMU.9101
P577
2003-01-01T00:00:00Z