4th Workshop of the European CMT-Consortium – 62nd ENMC International Workshop: Rare forms of Charcot-Marie-Tooth disease and related disorders. 16–18 October 1998, Soestduinen, The Netherlands-Reference-Cited by-同舟云学术

4th Workshop of the European CMT-Consortium – 62nd ENMC International Workshop: Rare forms of Charcot-Marie-Tooth disease and related disorders. 16–18 October 1998, Soestduinen, The Netherlands

Published:1999-06 Issue:4 Volume:9 Page:279-287
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Martin Jean-Jacques,Brice Alexis,Van Broeckhoven Christine

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference40 articles.

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2. Mutations in the early growth response 2 (EGR 2) gene are associated with hereditary myelinopathies;Warner;Nature Genet,1998

3. Clinicopathological and genetic study of patients with the Dejerine–Sottas phenotype;Parman;J Neurol,1998

4. Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood;Ouvrier;J Child Neurol,1996

5. Clinical phenotypes of different MPZ (P0) mutations may include Charcot–Marie–Tooth type 1B, Dejerine–Sottas, and congenital hypomyelination;Warner;Neuron,1996

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