NovelPRRT2mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes-Reference-Cited by-同舟云学术

NovelPRRT2mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes

Published:2012-12-21 Issue:2 Volume:12 Page:234-240
ISSN:1601-1848
Container-title:Genes, Brain and Behavior
language:en
Short-container-title:Genes, Brain and Behavior

Author:

Liu X.-R.¹,Wu M.¹,He N.¹,Meng H.¹,Wen L.¹,Wang J.-L.²,Zhang M.-P.³,Li W.-B.¹,Mao X.²,Qin J.-M.¹,Li B.-M.¹,Tang B.¹,Deng Y.-H.¹,Shi Y.-W.¹,Su T.¹,Yi Y.-H.¹,Tang B.-S.²,Liao W.-P.¹

Affiliation:

1. Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China; Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University; Guangzhou; China

2. Department of Neurology; Xiangya Hospital, Central South University; Changsha; China

3. Department of Pediatrics, Foshan Women and Children Hospital; Foshan; Guangdong; China

Publisher

Wiley

Subject

Behavioral Neuroscience,Neurology,Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/gbb.12008/fullpdf

Reference40 articles.

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2. Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria;Bruno;Neurology,2004

3. Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia;Bruno;Neurology,2007