Charcot–Marie–Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family-Reference-Cited by-同舟云学术

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Charcot–Marie–Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family

Published:2002-05 Issue:4 Volume:12 Page:399-404
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Santoro L.,Manganelli F.,Di Maio L.,Barbieri F.,Carella M.,D'Adamo P.,Casari G.

Publisher

Elsevier BV

Subject

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

Reference29 articles.

1. Hereditary motor and sensory neuropathies;Dyck,1993

2. The clinical features of hereditary motor and sensory neuropathy type I and II;Harding;Brain,1980

3. 2nd Workshop of the European CMT Consortium: 53rd ENMC International Workshop on Classification and Diagnostic Guidelines for Charcot–Marie–Tooth type 2 (CMT2-HMSN II) and Distal Hereditary Motor Neuropathy (Distal HMN-Spinal CMT), 26–28 September 1997, Naarden, The Netherlands;Brice;Neuromuscul Disord,1998

4. 3nd Workshop of the European CMT Consortium: 54rd ENMC International Workshop on Genotype/Phenotype Correlations in Charcot–Marie–Tooth type 1 and Hereditary Neuropathy with Liability to Pressure Palsies, 28–30 November 1997, Naarden, The Netherlands;De Jonghe;Neuromuscul Disord,1998

5. Localization of a gene (CMT2A) for autosomal dominant Charcot–Marie–Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity;Ben Othmane;Genomics,1993

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