Increased risk for recurrent major depression in DYT1 dystonia mutation carriers

Neurology

Volumn 63, Issue 4, 2004, Pages 631-637

  Heiman, Gary A ^a,f   Ottman, R ^a,b,d   Saunders Pullman, R J ^c   Ozelius, L J ^c   Risch, N J ^e   Bressman, S B ^c  

^a Columbia University ^*  (United States)

^b Taub Institute for Research on Alzheimer's Disease and the Aging Brain and the Gertrude H Sergievsky Center   (United States)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d NEW YORK STATE PSYCHIATRIC INSTITUTE   (United States)

^e STANFORD UNIVERSITY   (United States)

^f Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BIPOLAR DISORDER; BRAIN FUNCTION; CHROMOSOME 9Q; CHRONIC DISEASE; COMORBIDITY; DISEASE SEVERITY; DYSTONIA; DYT1 GENE; FEMALE; GENE; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENETIC RISK; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MAJOR DEPRESSION; MALE; PRIORITY JOURNAL; RECURRENT DISEASE;

EID: 4143083744     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000137113.39225.FA     Document Type: Article

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