Transient, Recurrent, White Matter Lesions in X-Linked Charcot-Marie-Tooth Disease With Novel Connexin 32 Mutation

Archives of Neurology
doi 10.1001/archneur.60.4.605
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Medical Association (AMA)

Related search

The First De Novo Mutation of the Connexin 32 Gene Associated With X Linked Charcot-Marie-Tooth Disease.

Journal of Medical Genetics
Genetics
1998English

X-Linked Charcot-Marie-Tooth Disease Type 3

2020English

A Novel GJB1 Mutation Associated With X‐linked Charcot–Marie–Tooth Disease in a Large Chinese Family Pedigree

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2020English

Charcot–Marie–Tooth Disease

2012English

A Novel p.Val244Leu Mutation in MFN2 Leads to Charcot-Marie-Tooth Disease Type 2

Italian Journal of Pediatrics
Child HealthPediatricsPerinatology
2016English

Charcot-Marie-Tooth Disease Type 2R

2020English

Update on Charcot-Marie-Tooth Disease

Current Neurology and Neuroscience Reports
NeuroscienceNeurology
2010English

Charcot-Marie-Tooth Disease Type 2B5

2020English

Mutation Screening of Mitofusin 2 in Charcot-Marie-Tooth Disease Type 2

Journal of Neurology
Neurology
2011English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy