Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34

Annals of Neurology

Volumn 27, Issue 2, 1990, Pages 114-120

  Kramer, Patricia L ^a   De Leon, Deborah ^b   Ozelius, Laurie ^a,d   Risch, Neil ^e   Bressman, Susan B ^b   Brin, Mitchell F ^b   Schuback, Deborah E ^c   Burke, Robert E ^b   Kwiatkowski, David J ^c   Shale, Heidi ^b   Gusella, James F ^a,d   Breakefield, Xandra O ^c,d,f   Fahn, Stanley ^b  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b Columbia University College of Physicians and Surgeons ^*  (United States)

^c MASSACHUSETTS GENERAL HOSPITAL   (United States)

^d HARVARD MEDICAL SCHOOL   (United States)

^e YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 9Q; DYSTONIA; ETHNIC OR RACIAL ASPECTS; HEREDITY; HUMAN; INHERITANCE; JEW; LINKAGE ANALYSIS; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 9; DYSTONIA MUSCULORUM DEFORMANS; FEMALE; HUMAN; JEWS; LINKAGE (GENETICS); MALE; MIDDLE AGE; PEDIGREE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0025238901     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.410270203     Document Type: Article

References (47)

1. Concepts and classification of dystonia
2. Inheritance of idiopathic torsion dystonia among Jews
3. The torsion dystonias: literature review: genetic and clinical studies
4. Dystonia musculorum deformans: clinical genetic and pathoanatomical studies
5. Human gene for torsion dystonia located on chromosome 9q32‐34
6. Human gene for torsion dystonia located on chromosome 9q32‐34
7. The molecular genetics of an autosomal dominant form of torsion dystonia
8. Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance
9. Torsion dystonia in Panay, Philippines
10. X‐linked recessive dystonia and parkinsonism in Filipino males
11. Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro‐opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphisms
12. Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q and 21q by multi‐point linkage analysis
13. Addendum to “A technique for radiolabeling DNA restriction fragments to high specific activity
14. Dispersion of argininosuccinate‐synthetase‐like human genes to multiple autosomes and the X Chromosome
15. Multilocus linkage analysis with the human argininosuccinate synthetase gene
16. Isolation and mapping of a polymorphic DNA sequence pMCT136 on chromosome 9q (D9S10)
17. A mapped set of genetic markers for human chromosome 9
18. A genetic linkage map of the human genome
19. Localization of gelsolin proximal to ABL on chromosome 9
20. The gelsolin cDNA clone from 9q32‐34 identifies BclI and Stul RFLPs
21. An anonymous DNA probe (Lamp92) detects a PvuII polymorphism on human chromosome 9 (D9S29)
22. 1‐acid glycoprotein to 9q31‐q32
23. Report of the committee on the genetic constitution of chromosomes 7, 8 and 9
24. Report of the committee on the genetic constitution of chromosome 9 and 10
25. Use of cyclosporin A in establishing Epstein‐Barr Virus–transformed human lymphoblastoid cell lines
26. Precise localization of human beta‐globin gene complex on chromosome 11
27. Gel electrophoresis of restriction fragments
28. Age‐of‐onset correction available for linkage analysis (LIPED)
29. A Computer Program for linkage analysis of general human pedigrees
30. Genetic linkage map of human chromosome 21
31. Efficient Computations in multi‐locus linkage analysis
32. Mapmaker: an interactive computer package for constructing primary genetic linkage map of experimental and natural populations
33. A new statistical test for linkage heterogeneity
34. Generalized dystonia: concept and treatment
35. Autosomal dominant torsion dystonia in a Swedish family
36. Long‐term treatment with levodopa in a family with autosomal dominant torsion dystonia
37. Dopa‐responsive dystonia
38. Hereditary progressive dystonia with marked diurnal fluctuation
39. Paroxysmal non‐kinesigenic dystonia
40. Hereditary myoclonic dystonia, hereditary torsion dystonia and hereditary essential myoclonus: an area of confusion
41. Myoclonus and dystonia: a family study