Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions-Reference-Cited by-同舟云学术

Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions

Published:2012-01 Issue:1 Volume:1 Page:2-12
ISSN:2211-1247
Container-title:Cell Reports
language:en
Short-container-title:Cell Reports

Author:

Lee Hsien-Yang,Huang Yong,Bruneau Nadine,Roll Patrice,Roberson Elisha D.O.,Hermann Mark,Quinn Emily,Maas James,Edwards Robert,Ashizawa Tetsuo,Baykan Betul,Bhatia Kailash,Bressman Susan,Bruno Michiko K.,Brunt Ewout R.,Caraballo Roberto,Echenne Bernard,Fejerman Natalio,Frucht Steve,Gurnett Christina A.,Hirsch Edouard,Houlden Henry,Jankovic Joseph,Lee Wei-Ling,Lynch David R.,Mohammed Shehla,Müller Ulrich,Nespeca Mark P.,Renner David,Rochette Jacques,Rudolf Gabrielle,Saiki Shinji,Soong Bing-Wen,Swoboda Kathryn J.,Tucker Sam,Wood Nicholas,Hanna Michael,Bowcock Anne M.,Szepetowski Pierre,Fu Ying-Hui,Ptáček Louis J.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference44 articles.

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2. A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16;Bennett;Neurology,2000

3. Paroxysmal dyskinesias;Bhatia;Mov. Disord.,2011

4. Secondary paroxysmal dyskinesias;Blakeley;Mov. Disord.,2002

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

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