Author:
Vandervore Laura V.,Schot Rachel,Milanese Chiara,Smits Daphne J.,Kasteleijn Esmee,Fry Andrew E.,Pilz Daniela T.,Brock Stefanie,Börklü-Yücel Esra,Post Marco,Bahi-Buisson Nadia,Sánchez-Soler María José,van Slegtenhorst Marjon,Keren Boris,Afenjar Alexandra,Coury Stephanie A.,Tan Wen-Hann,Oegema Renske,de Vries Linda S.,Fawcett Katherine A.,Nikkels Peter G.J.,Bertoli-Avella Aida,Al Hashem Amal,Alwabel Abdulmalik A.,Tlili-Graiess Kalthoum,Efthymiou Stephanie,Zafar Faisal,Rana Nuzhat,Bibi Farah,Houlden Henry,Maroofian Reza,Person Richard E.,Crunk Amy,Savatt Juliann M.,Turner Lisbeth,Doosti Mohammad,Karimiani Ehsan Ghayoor,Saadi Nebal Waill,Akhondian Javad,Lequin Maarten H.,Kayserili Hülya,van der Spek Peter J.,Jansen Anna C.,Kros Johan M.,Verdijk Robert M.,Milošević Nataša Jovanov,Fornerod Maarten,Mastroberardino Pier Giorgio,Mancini Grazia M.S.
Funder
COST
Steunfonds Marguerite-Marie Delacroix
FWO
Newlife Foundation for Disabled Children
Wales Epilepsy Research Network
Wales Gene Park
ZonMW
The Wellcome Trust
Synaptopathies
National Institute for Health Research University College London Hospitals Biomedical Research Centre
Medical Research Council
the National Institute for Health Research University College London Hospitals Biomedical Research Centre
Rosetree Trust
Ataxia UK
Multiple System Atrophy (MSA) Trust
Brain Research UK
Sparks Great Ormand Street Hospital (GOSH) Charity
Muscular Dystrophy UK
Muscular Dystrophy Association
Subject
Genetics(clinical),Genetics