A study of idiopathic torsion dystonia in a non-Jewish family: evidence for genetic heterogeneity.

Bressman, S B; Heiman, G A; Nygaard, T G; Ozelius, L J; Hunt, A L; Brin, M F; Gordon, M F; Moskowitz, C B; de Leon, D; Burke, R E

Bressman, S B; Heiman, G A; Nygaard, T G; Ozelius, L J; Hunt, A L; Brin, M F; Gordon, M F; Moskowitz, C B; de Leon, D; Burke, R E.

Affiliation

Bressman SB; Department of Neurology, Columbia-Presbyterian Medical Center, New York, NY 10032.

Neurology ; 44(2): 283-7, 1994 Feb.

Article in En | MEDLINE | ID: mdl-8309575

Subject(s)

Chromosomes, Human, Pair 9; Dystonia Musculorum Deformans/genetics; Adolescent; Adult; Age of Onset; Child; Christianity; Chromosome Mapping; Dystonia Musculorum Deformans/diagnosis; Dystonia Musculorum Deformans/physiopathology; Family; Female; Genetic Carrier Screening; Genetic Linkage; Genetic Markers; Germany/ethnology; Humans; Jews/genetics; Lod Score; Male; Middle Aged; North America; Pedigree

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Database: MEDLINE Main subject: Chromosomes, Human, Pair 9 / Dystonia Musculorum Deformans Type of study: Diagnostic_studies Limits: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Country/Region as subject: America do norte / Europa Language: En Year: 1994 Type: Article

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