A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia-Reference-Cited by-同舟云学术

A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia

Published:2015-06 Issue:6 Volume:96 Page:938-947
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Mencacci Niccolo E.,Rubio-Agusti Ignacio,Zdebik Anselm,Asmus Friedrich,Ludtmann Marthe H.R.,Ryten Mina,Plagnol Vincent,Hauser Ann-Kathrin,Bandres-Ciga Sara,Bettencourt Conceição,Forabosco Paola,Hughes Deborah,Soutar Marc M.P.,Peall Kathryn,Morris Huw R.,Trabzuni Daniah,Tekman Mehmet,Stanescu Horia C.,Kleta Robert,Carecchio Miryam,Zorzi Giovanna,Nardocci Nardo,Garavaglia Barbara,Lohmann Ebba,Weissbach Anne,Klein Christine,Hardy John,Pittman Alan M.,Foltynie Thomas,Abramov Andrey Y.,Gasser Thomas,Bhatia Kailash P.,Wood Nicholas W.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference56 articles.

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