Influence of comorbidities on the phenotype of patients affected by Charcot–Marie–Tooth neuropathy type 1A-Reference-Cited by-同舟云学术

Influence of comorbidities on the phenotype of patients affected by Charcot–Marie–Tooth neuropathy type 1A

Published:2013-11 Issue:11 Volume:23 Page:902-906
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Ursino Giulia,Alberti M. Antonia,Grandis Marina,Reni Lizia,Pareyson Davide,Bellone Emilia,Gemelli Chiara,Sabatelli Mario,Pisciotta Chiara,Luigetti Marco,Santoro Lucio,Massollo Laura,Schenone Angelo

Publisher

Elsevier BV

Subject

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

Reference24 articles.

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2. Estimation of the mutation frequencies in Charcot–Marie–Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study;Nelis;Eur J Hum Genet,1996

3. DNA duplication associated with Charcot–Marie–Tooth disease type 1A;Lupski;Cell,1991

4. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot–Marie–Tooth disease type 1A;Patel;Nat Genet,1992

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

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