A new truncating MPZ mutation associated with a very mild CMT1 B phenotype-Reference-Cited by-同舟云学术

A new truncating MPZ mutation associated with a very mild CMT1 B phenotype

Published:2010-12 Issue:12 Volume:20 Page:817-819
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Piazza Selina,Baldinotti Fulvia,Fogli Antonella,Conidi Maria Elena,Michelucci Angela,Ienco Elena Caldarazzo,Mancuso Michelangelo,Simi Paolo,Siciliano Gabriele

Publisher

Elsevier BV

Subject

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

Reference19 articles.

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4. The peripheral myelin protein gene PMP22 is contained within the Charcot–Marie–Tooth disease type 1A duplication;Timmerman;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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