Mutations in the sodium channel Nav1.7 underlie inherited erythromelalgia
Author:
Publisher
Elsevier BV
Subject
Drug Discovery,Molecular Medicine
Reference40 articles.
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4. Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia;Burns;Br. J. Dermatol.,2005
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