Molecular Diagnosis of Charcot-Marie Tooth Disease
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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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2002-02-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/1659 |