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Sensory Evaluation of the Hands in Patients with Charcot-Marie-Tooth Disease Using Semmes-Weinstein Monofilaments

✍ Scribed by Ton A.R. Schreuders; Ruud W. Selles; Berbke T.J. van Ginneken; Wim G.M. Janssen; Henk J. Stam


Book ID
118728249
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
473 KB
Volume
21
Category
Article
ISSN
0894-1130

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In a previous study, we have shown that N-myc downstream-regulated gene 1 (NDRG1), classified in databases as a tumor suppressor and heavy metal-response protein, is mutated in hereditary motor and sensory neuropathy Lom (HMSNL), a severe autosomal recessive form of Charcot-Marie-Tooth (CMT) disease