Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene-Reference-Cited by-同舟云学术

Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene

Published:2004-04 Issue:4 Volume:14 Page:261-264
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Stojkovic Tanya,Latour Philippe,Viet Ghislaine,de Seze Jérôme,Hurtevent Jean-François,Vandenberghe Antoon,Vermersch P.

Publisher

Elsevier BV

Subject

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

Reference19 articles.

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4. N-myc-downstream regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom;Kalaydjieva;Am J Hum Genet,2000

5. A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charot-Marie-Tooth disease;Guilbot;Hum Mol Genet,2001

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