Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients-Reference-Cited by-同舟云学术

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients

Published:2003-01-01 Issue:1 Volume:126 Page:134-151
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Hattori N.,Yamamoto M.,Yoshihara T.,Koike H.,Nakagawa M.,Yoshikawa H.,Ohnishi A.,Hayasaka K.,Onodera O.,Baba M.,Yasuda H.,Saito T.,Nakashima K.,Kira J.-i.,Kaji R.,Oka N.,Sobue G.,Study Group for Hereditary Neuropathy

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/126/1/134/848484/awg012.pdf

Reference78 articles.

1. Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

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3. Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

4. Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: A 20-year study

5. Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases

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