An axonal form of Charcot-Marie-Tooth disease with a novel missense mutation in the myelin protein zero gene

An axonal form of Charcot-Marie-Tooth disease with a novel missense mutation in the myelin protein zero gene

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Bibliographic Details
Published in:Journal of the peripheral nervous system Vol. 9; no. 1; pp. 1 - 2
Main Authors: Kochanski, Andrzej, Kabzinska, Dagmara, Nowakowski, Adam, Drac, Hanna, Hausmanowa-Petrusewicz, Irena
Format: Journal Article
Language:English
Published: Oxford, UK; Malden , USA Blackwell Science Inc 01-03-2004
Subjects:
Adult
Axons - pathology
Charcot-Marie-Tooth Disease - genetics
Charcot-Marie-Tooth Disease - pathology
Female
Humans
Mutation, Missense
Myelin P0 Protein - genetics
Polymorphism, Single-Stranded Conformational
Online Access:Get full text
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Description
Bibliography:ArticleID:JNS509101
ark:/67375/WNG-VL72P2KG-P
istex:F5DB7F3D84F2F022CA2F51AD67AC25AE17999A04
ISSN:1085-9489
1529-8027
DOI:10.1111/j.1085-9489.2004.09101.x