Molecular Diagnosis of Charcot-Marie Tooth Disease
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.
DOI: https://doi.org/10.15844/pedneurbriefs-16-2-1 | Journal eISSN: 2166-6482
Language: English
Page range: 9 - 9
Published on: Feb 1, 2002
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2002 J. Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.