DCTN1 mutations in Perry syndrome

Nature Genetics

Volumn 41, Issue 2, 2009, Pages 163-165

  Farrer, Matthew J ^a   Hulihan, Mary M ^a   Kachergus, Jennifer M ^a   Dächsel, Justus C ^a   Stoessl, A Jon ^b   Grantier, Linda L ^b   Calne, Susan ^b   Calne, Donald B ^b   Lechevalier, Bernard ^c   Chapon, Francoise ^c   Tsuboi, Yoshio ^d   Yamada, Tatsuo ^d   Gutmann, Ludwig ^e   Elibol, Bülent ^f   Bhatia, Kailash P ^g   Wider, Christian ^a   Vilarĩo Güell, Carles ^a   Ross, Owen A ^a   Brown, Laura A ^a   Castanedes Casey, Monica ^a   Dickson, Dennis W ^a   Wszolek, Zbigniew K ^a   more..

^a MAYO CLINIC   (United States)

^b Pacific Parkinson's Research Centre   (Canada)

^c CAEN UNIVERSITY HOSPITAL   (France)

^d FUKUOKA UNIVERSITY   (Japan)

^e WEST VIRGINIA UNIVERSITY   (United States)

^f HACETTEPE UNIVERSITY   (Turkey)

^g UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSKELETON ASSOCIATED PROTEIN GLYCINE RICH; DNA; DYNACTIN; GLYCINE; PROTEIN; TAR DNA BINDING PROTEIN; UNCLASSIFIED DRUG;

ADULT; ARTICLE; BINDING AFFINITY; BRAIN DISEASE; CELL INCLUSION; CELL POPULATION; CLINICAL ARTICLE; CONTROLLED STUDY; DEPRESSION; DISEASE ASSOCIATION; FEMALE; GENE FUNCTION; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; HETEROZYGOTE; HUMAN; HUMAN TISSUE; HYPOVENTILATION; IMMUNOHISTOCHEMISTRY; LINKAGE ANALYSIS; MALE; MICROTUBULE; MOTOR NEURON DISEASE; MUTATIONAL ANALYSIS; PARKINSONISM; PERRY SYNDROME; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN MOTIF; SYNDROME; WEIGHT REDUCTION;

BRAIN; DEPRESSION; DNA-BINDING PROTEINS; FAMILY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; HYPOVENTILATION; MALE; MICROTUBULE-ASSOCIATED PROTEINS; MUTATION; PARKINSONIAN DISORDERS; PEDIGREE; SYNDROME; WEIGHT LOSS;

EID: 59149097039     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.293     Document Type: Article

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