EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy

EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy

Item
http://www.wikidata.org/entity/Q28214469
Q28182289
sameAs
Characteristics of demyelinating Charcot-Marie-Tooth disease with concurrent diabetes mellitus.Signals that determine Schwann cell identity.Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease.Molecular diagnostics of Charcot-Marie-Tooth disease and related peripheral neuropathies.Paradoxical role of an Egr transcription factor family member, Egr2/Krox20, in learning and memoryDemyelinating prenatal and infantile developmental neuropathies.Autosomal recessive Charcot-Marie-Tooth disease: from genes to phenotypes.Pluripotent stem cells for Schwann cell engineering.The Ddx20/DP103 dead box protein represses transcriptional activation by Egr2/Krox-20.Vincristine exacerbates asymptomatic Charcot-Marie-tooth disease with a novel EGR2 mutation.Clinico-pathologic conference: congenital hypomyelinating neuropathy in two infants of a triplet birth.Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy.EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome.
P2860

EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy

Item
http://www.wikidata.org/entity/Q28214469
description
2001 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2001
@ast
scientific article (publication date: July 2001)
@en
vedecký článok (publikovaný 2001-07)
@sk
vědecký článek publikovaný v roce 2001
@cs
wetenschappelijk artikel (gepubliceerd in 2001-07)
@nl
wissenschaftlicher Artikel
@de
наукова стаття, опублікована в липні 2001
@uk
مقالة علمية (نشرت في يوليو 2001)
@ar
name
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
@ast
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
@en
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
@nl
type
label
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
@ast
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
@en
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
@nl
prefLabel
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
@ast
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
@en
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
@nl
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P577
P698
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P1433
P1476
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
@en
P2093
P2888
P304
P31
P356
P407
P433
P478
P577
P698