A Multi-center Genome-wide Association Study of Cervical Dystonia.
Yan V Sun,Chengchen Li,Qin Hui,Yunfeng Huang,Richard Barbano,Ramon Rodriguez,Irene A Malaty,Stephen Reich, Kimberly Bambarger, Katie Holmes,Joseph Jankovic,Neepa J Patel,Emmanuel Roze,Marie Vidailhet,Brian D Berman,Mark S LeDoux,Alberto J Espay,Pinky Agarwal,Sarah Pirio-Richardson,Samuel A Frank,William G Ondo,Rachel Saunders-Pullman,Sylvain Chouinard,Stover Natividad,Alfredo Berardelli,Alexander Y Pantelyat,Allison Brashear,Susan H Fox,Meike Kasten,Ulrike M Krämer,Miriam Neis,Tobias Bäumer,Sebastian Loens,Max Borsche,Simone Zittel, Antonia Maurer,Mathias Gelderblom,Jens Volkmann,Thorsten Odorfer,Andrea A Kühn,Friederike Borngräber,Inke R König,Carlos Cruchaga,Adam C Cotton,Gamze Kilic-Berkmen,Alan Freeman,Stewart A Factor,Laura Scorr,J Douglas Bremner,Viola Vaccarino,Arshed A Quyyumi,Christine Klein,Joel S Perlmutter,Katja Lohmann,Hyder A Jinnah Movement disorders : official journal of the Movement Disorder Society（2021）
摘要
The genetic underpinnings of cervical dystonia are complex and likely consist of multiple distinct variants of small effect sizes. Larger sample sizes may be needed to provide sufficient statistical power to address the presumably multi-genic etiology of cervical dystonia. © 2021 International Parkinson and Movement Disorder Society.
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关键词
cervical dystonia,genome-wide association study (GWAS),movement disorder,rare disease
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