Molecular Diagnosis of Charcot-Marie Tooth Disease

Authors

  • J. Gordon Millichap Departments of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL

DOI:

https://doi.org/10.15844/pedneurbriefs-16-2-1

Keywords:

Charcot-Marie-Tooth, Sporadic Neuropathy, Clinical Diagnosis

Abstract

The frequency of mutations in certain genes in 153 unrelated patients with Charcot-Marie-Tooth disease (CMT) was determined by DNA sequencing before clinical testing at the Departments of Molecular and Human Genetics and Pediatrics, Baylor College of Medicine, Houston, TX, and other centers.

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Published

2002-02-01

Issue

Vol 16, No 02 | Feb 2002

Section

Neuromuscular Disorders

License

Copyright (c) 2002 The Author(s)

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