Huntington disease-like phenotype in a patient with ANO3 mutation
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference14 articles.
1. A novel ANO3 variant identified in a 53-year-old woman presenting with hyperkinetic dysarthria, blepharospasm, hyperkinesias, and complex motor tics;Blackburn;BMC Med. Genet.,2016
2. Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis;Charlesworth;Am. J. Hum. Genet.,2012
3. Spatio-temporal transcriptome of the human brain;Kang;Nature,2011
4. Structure and function of tmem16 proteins (anoctamins);Pedemonte;Physiol. Rev.,2014
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