Two novel missense mutations in the myelin protein zero gene causes Charcot-Marie-Tooth type 2 and Déjérine-Sottas syndrome

Two novel missense mutations in the myelin protein zero gene causes Charcot-Marie-Tooth type 2 and Déjérine-Sottas syndrome

<p>Abstract</p> <p>Background</p> <p>The Charcot-Marie-Tooth (CMT) phenotype caused by mutation in the <it>myelin protein zero (MPZ) </it>gene varies considerably, from early onset and severe forms to late onset and milder forms. The mechanism is not well un...

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Bibliographic Details
Main Authors: Sand Jette C, Braathen Geir J, Russell Michael B
Format: Article
Language:English
Published: BMC 2010-04-01
Series:BMC Research Notes
Online Access:http://www.biomedcentral.com/1756-0500/3/99

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