Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation.
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Dominant GDAP1 mutations cause predominantly mild CMT phenotypesNeuropathy-Associated Egr2 Mutants Disrupt Cooperative Activation of Myelin Protein Zero by Egr2 and Sox10Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathiesDifferential regulation of NAB corepressor genes in Schwann cells.The molecular machinery of myelin gene transcription in Schwann cells.TRPV4 mutations in children with congenital distal spinal muscular atrophy.Locus-wide identification of Egr2/Krox20 regulatory targets in myelin genesClinical and electrophysiological aspects of Charcot-Marie-Tooth disease.Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.Inherited peripheral neuropathies.Paradoxical role of an Egr transcription factor family member, Egr2/Krox20, in learning and memoryInteractions of Sox10 and Egr2 in myelin gene regulationCharcot-Marie-Tooth disease: a clinico-genetic confrontation.Laryngeal neuropathy of Charcot-Marie-Tooth disease: further observations and novel mutations associated with vocal fold paresis.Demyelinating prenatal and infantile developmental neuropathies.In vivo detection of Egr2 binding to target genes during peripheral nerve myelination.Vocal cord paralysis in Charcot-Marie-Tooth type 4b1 disease associated with a novel mutation in the myotubularin-related protein 2 gene: A case report and review of the literatureRegulation of cholesterol/lipid biosynthetic genes by Egr2/Krox20 during peripheral nerve myelination.The Ddx20/DP103 dead box protein represses transcriptional activation by Egr2/Krox-20.Blink reflex role in algorithmic genetic testing of inherited polyneuropathies.Genetic epidemiology of Charcot-Marie-Tooth disease.Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families
P2860
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P2860
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation.
description
2000 nî lūn-bûn
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2000 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2000年の論文
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2000年論文
@yue
2000年論文
@zh-hant
2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
Cranial nerve involvement in C ...... owth response 2 gene mutation.
@ast
Cranial nerve involvement in C ...... owth response 2 gene mutation.
@en
type
label
Cranial nerve involvement in C ...... owth response 2 gene mutation.
@ast
Cranial nerve involvement in C ...... owth response 2 gene mutation.
@en
prefLabel
Cranial nerve involvement in C ...... owth response 2 gene mutation.
@ast
Cranial nerve involvement in C ...... owth response 2 gene mutation.
@en
P2093
P50
P356
P1433
P1476
Cranial nerve involvement in C ...... owth response 2 gene mutation.
@en
P2093
P304
P356
10.1212/WNL.54.8.1696
P407
P577
2000-04-01T00:00:00Z