A major locus for several phenotypes of myoclonus-dystonia on chromosome 7q

Neurology

Volumn 56, Issue 9, 2001, Pages 1213-1216

  Vidailhet, M ^a,b   Tassin, J ^a   Durif, F ^c   Nivelon Chevallier, A ^d   Agid, Y ^a   Brice, Alexis ^a   Durr A ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b HÔPITAL SAINT ANTOINE   (France)

^c SERVICE DE RHUMATOLOGIE   (France)

^d Hôpital Enfants du Bocage   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DOPAMINE 2 RECEPTOR;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CHROMOSOME 11; CHROMOSOME 7Q; CHROMOSOME MUTATION; CLINICAL ARTICLE; DYSTONIA; FEMALE; GENE LOCUS; GENETIC LINKAGE; HUMAN; MALE; MYOCLONUS; PHENOTYPE; PRIORITY JOURNAL;

EID: 0035826884     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.56.9.1213     Document Type: Article

References (10)

1. Essential myoclonus and myoclonic dystonia
2. Inherited myoclonus-dystonia syndrome
3. Association of a missense change in the D2 dopamine receptor with myoclonus dystonia
4. Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31
5. Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia
6. D2 dopamine receptor gene in myoclonic dystonia and essential myoclonus
7. A comprehensive map of the human genome based on 5,264 microsatellites
8. Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
9. Avoiding recomputation in genetic linkage analysis
10. A major locus for myoclonus-dystonia maps to chromosome 7q in eight families