Authors: 1097-4199 Article; ar scopus.relation.lastpage; scopus.subject.keywords; scopus.relation.firstpage; scopus.description.allpeopleoriginal; scopus.description.abstract; scopus.language.iso

Journal: 109

Conference: amyotrophic lateral sclerosis; frontotemporal dementia; huntingtin; repeat expansions; whole-genome sequencing;

Publisher: 3

Published: 100001671 - Hereditary Disease Foundation; 100000051 - National Human Genome Research Institute; 501100000272 - National Institute for Health and Care Research; 100000002 - National Institutes of Health; 501100000780 - European Commission; 100013352 - Tow Foundation; 100016012 - Huntington's Disease Society of America; 100019850 - Cerevel Therapeutics; 100000049 - National Institute on Aging; 100000049 - National Institute on Aging; 100000738 - U.S. Department of Veterans Affairs; 100000738 - U.S. Department of Veterans Affairs; 100014013 - UK Research and Innovation; 100014013 - UK Research and Innovation; 501100000265 - Medical Research Council; 501100000265 - Medical Research Council; 100011102 - Seventh Framework Programme; 100011102 - Seventh Framework Programme; 100000065 - National Institute of Neurological Disorders and Stroke; 100000065 - National Institute of Neurological Disorders and Stroke; 100000050 - National Heart, Lung, and Blood Institute; 100000050 - National Heart, Lung, and Blood Institute; 100000971 - ALS Association; 100000971 - ALS Association; 100010269 - Wellcome Trust; 100010269 - Wellcome Trust; 501100003196 - Ministero della Salute; 501100003196 - Ministero della Salute;

DOI: eng

Volume: 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