Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

Movement Disorders

Volumn 31, Issue 4, 2016, Pages 436-457

  Marras, Connie ^a   Lang, Anthony ^a   van de Warrenburg, Bart P ^b   Sue, Carolyn M ^c   Tabrizi, Sarah J ^d   Bertram, Lars ^e,f   Mercimek Mahmutoglu, Saadet ^g   Ebrahimi Fakhari, Darius ^h,i   Warner, Thomas T ^j   Durr, Alexandra ^k   Assmann, Birgit ^h   Lohmann, Katja ^e   Kostic, Vladimir ^l   Klein, Christine ^e  

^a UNIVERSITY OF TORONTO   (Canada)

^b RADBOUD UNIVERSITY   (Netherlands)

^c UNIVERSITY OF SYDNEY   (Australia)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

^e UNIVERSITY OF LÜBECK   (Germany)

^f IMPERIAL COLLEGE LONDON   (United Kingdom)

^g HOSPITAL FOR SICK CHILDREN   (Canada)

^h UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

ⁱ BOSTON CHILDREN S HOSPITAL   (United States)

^j UNIVERSITY COLLEGE LONDON   (United Kingdom)

^k SORBONNE UNIVERSITÉ   (France)

^l UNIVERSITY OF BELGRADE   (Serbia)

more..

Author keywords

Genetics; Movement disorders; Nomenclature

Indexed keywords

ATAXIA; BRAIN CALCIFICATION; CHOREA; DYSTONIA; GENE; GENE NOMENCLATURE; GENE NUMBER; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC MOVEMENT DISORDER; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MEDICAL SOCIETY; MOTOR DYSFUNCTION; NEURODEGENERATION WITH BRAIN IRON ACCUMULATION; PARKINSONISM; PATHOGENESIS; PHENOTYPE; PRIMARY FAMILIAL BRAIN CALCIFICATION; PRIORITY JOURNAL; REVIEW; RISK FACTOR; SPASTIC PARAPLEGIA; CLASSIFICATION; GENETICS; STANDARDS;

HUMANS; MOVEMENT DISORDERS; SOCIETIES, MEDICAL;

EID: 84963550642     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.26527     Document Type: Review

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