HINT1mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia
Author:
Affiliation:
1. The Canadian Pharmacogenomic Network for Drug Safety (CPNDS), Center for Molecular Medicine and Therapeutics, Department of Medical Genetics; University of British Columbia; 950 West 28th Avenue; Vancouver; BC; V5Z4H4; Canada.
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference2 articles.
1. Genetic and clinical aspects of Charcot-Marie-Tooth's disease;Skre;Clin Genet,1974
2. Neuromyotonia;P;Clin Neurophysiol,2006
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