PRRT2 c.649dupC Mutation Derived from De Novo in Paroxysmal Kinesigenic Dyskinesia.

CONCLUSION: These findings demonstrate the heterogeneity of PKD, and the de novo mutagenesis of PRRT2 gene might indicate the genetic instability of this region. PMID: 23176561 [PubMed - in process]

http://www.ncbi.nlm.nih.gov/PubMed/23176561?dopt=Abstract

Source: CNS Neuroscience and Therapeutics - January 1, 2013 Category: Neuroscience Authors: Li HF, Ni W, Xiong ZQ, Xu J, Wu ZY Tags: CNS Neurosci Ther Source Type: research