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Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

✍ Scribed by Baxter, Rachel V.; Ben Othmane, Kamel; Rochelle, Julie M.; Stajich, Jason E.; Hulette, Christine; Dew-Knight, Susan; Hentati, Faycal; Ben Hamida, Mongi; Bel, S.; Stenger, Judy E.

Book ID: 109919696
Publisher: Nature Publishing Group
Year: 2001
Tongue: English
Weight: 300 KB
Volume: 30
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng796

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Hereditary motor and sensory neuropathies (HMSN) comprises a wide clinical spectrum of related disorders with defects in peripheral nerve myelination. Charcot-Marie-Tooth type 1 (CMT1) is the most common form and is usually a mild disease with onset in the first or second decade; however there is a