Communicated by Jean-Louis Mandel Charcot-Marie-Tooth type 1 (CMT1) disease is an autosomal dominant neuropathy of the peripheral nerve. The majority of CMT 1 cases are due to a duplication of an 1.5-Mb DNA fragment on chromosome 17pl1.2 (CMT la). Micromutations were found in the gene for peripheral
โฆ LIBER โฆ
Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero gene
โ Scribed by Marrosu, M. G.; Vaccargiu, S.; Marrosu, G.; Vannelli, A.; Cianchetti, C.; Muntoni, F.
- Book ID
- 115450367
- Publisher
- Lippincott Williams and Wilkins
- Year
- 1998
- Tongue
- English
- Weight
- 634 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0028-3878
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