X-linked dominant Charcot–Marie–Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations-Reference-Cited by-同舟云学术

X-linked dominant Charcot–Marie–Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations

Published:1999-08 Issue:2 Volume:167 Page:90-101
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Senderek Jan,Hermanns Benita,Bergmann Carsten,Boroojerdi Babak,Bajbouj Malek,Hungs Marcel,Ramaekers Vincent T.,Quasthoff Stefan,Karch Dieter,Schröder J.Michael

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference66 articles.

1. Hereditary motor and sensory neuropathies;Dyck,1993

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

3. Duplication in chromosome 17p11.2 in Charcot–Marie–Tooth neuropathy type 1a (CMT1a);Raeymaekers;Neuromusc Disord,1991

4. Identical point mutations of PMP22 in Trembler-J mouse and Charcot–Marie–Tooth disease type 1A;Valentijn;Nat Genet,1992

5. Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene;Hayasaka;Nat Genet,1993

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