Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B-Reference-Cited by-同舟云学术

Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B

Published:1995 Issue:1 Volume:6 Page:50-54
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Latour Philippe,Blanquet Françoise,Nelis Eva,Bonnebouche Christine,Chapon Fraņoise,Diraison Philippe,Ollagnon Elisabeth,Dautigny André,Pham-Dinh Danielle,Chazot Guy,Boucherat Michel,Van Broeckhoven Christine,Vandenberghe Antoon

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference27 articles.

1. Diagnostic criteria for autosomal dominant hereditary motor and sensory neuropathy type Ia

2. Dideoxy sequencing method using denatured plasmid templates

3. Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

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2. Impaired Mitochondrial Mobility in Charcot-Marie-Tooth Disease;Frontiers in Cell and Developmental Biology;2021-02-01

3. The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study;Clinical Neurophysiology;2018-01

4. Genotype–phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in theMPZgene;Brain;2015-08-25

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