The intramembrane COOH-terminal domain of PRRT2 regulates voltage-dependent Na+ channels
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference64 articles.
1. Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia;Chen;Nat. Genet.,2011
2. Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions;Lee;Cell Rep.,2012
3. The evolving spectrum of PRRT2-associated paroxysmal diseases;Ebrahimi-Fakhari;Brain,2015
4. The clinical and genetic heterogeneity of paroxysmal dyskinesias;Gardiner;Brain,2015
5. Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy;Heron;J. Med. Genet.,2013
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