201 related articles for article (PubMed ID: 7647798)
1. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1.
Benomar A; Krols L; Stevanin G; Cancel G; LeGuern E; David G; Ouhabi H; Martin JJ; Dürr A; Zaim A
Nat Genet; 1995 May; 10(1):84-8. PubMed ID: 7647798
[TBL] [Abstract][Full Text] [Related]
2. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I.
Benomar A; Le Guern E; Dürr A; Ouhabi H; Stevanin G; Yahyaoui M; Chkili T; Agid Y; Brice A
Ann Neurol; 1994 Apr; 35(4):439-44. PubMed ID: 8154871
[TBL] [Abstract][Full Text] [Related]
3. The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.
David G; Giunti P; Abbas N; Coullin P; Stevanin G; Horta W; Gemmill R; Weissenbach J; Wood N; Cunha S; Drabkin H; Harding AE; Agid Y; Brice A
Am J Hum Genet; 1996 Dec; 59(6):1328-36. PubMed ID: 8940279
[TBL] [Abstract][Full Text] [Related]
4. Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.
Verbeek DS; Schelhaas JH; Ippel EF; Beemer FA; Pearson PL; Sinke RJ
Hum Genet; 2002 Oct; 111(4-5):388-93. PubMed ID: 12384780
[TBL] [Abstract][Full Text] [Related]
5. A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.
Vahedi K; Joutel A; Van Bogaert P; Ducros A; Maciazeck J; Bach JF; Bousser MG; Tournier-Lasserve E
Ann Neurol; 1995 Mar; 37(3):289-93. PubMed ID: 7695228
[TBL] [Abstract][Full Text] [Related]
6. Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.
Li M; Ishikawa K; Toru S; Tomimitsu H; Takashima M; Goto J; Takiyama Y; Sasaki H; Imoto I; Inazawa J; Toda T; Kanazawa I; Mizusawa H
J Hum Genet; 2003; 48(3):111-8. PubMed ID: 12624721
[TBL] [Abstract][Full Text] [Related]
7. A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan.
Takashima M; Ishikawa K; Nagaoka U; Shoji S; Mizusawa H
J Hum Genet; 2001; 46(4):167-71. PubMed ID: 11322654
[TBL] [Abstract][Full Text] [Related]
8. North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysis.
Small KW; Udar N; Yelchits S; Klein R; Garcia C; Gallardo G; Puech B; Puech V; Saperstein D; Lim J; Haller J; Flaxel C; Kelsell R; Hunt D; Evans K; Lennon F; Pericak-Vance M
Mol Vis; 1999 Dec; 5():38. PubMed ID: 10617775
[TBL] [Abstract][Full Text] [Related]
9. Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2).
Dürr A; Brice A; Lepage-Lezin A; Cancel G; Smadja D; Vernant JC; Agid Y
Clin Neurosci; 1995; 3(1):12-6. PubMed ID: 7614088
[TBL] [Abstract][Full Text] [Related]
10. Best's vitelliform dystrophy (VMD2) maps between D11S903 and PYGM: no evidence for locus heterogeneity.
Weber BH; Walker D; Müller B; Mar L
Genomics; 1994 Mar; 20(2):267-74. PubMed ID: 8020974
[TBL] [Abstract][Full Text] [Related]
11. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.
Gispert S; Twells R; Orozco G; Brice A; Weber J; Heredero L; Scheufler K; Riley B; Allotey R; Nothers C
Nat Genet; 1993 Jul; 4(3):295-9. PubMed ID: 8358438
[TBL] [Abstract][Full Text] [Related]
12. Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1.
Krols L; Martin JJ; David G; Van Regemorter N; Benomar A; Löfgren A; Stevanin G; Dürr A; Brice A; Van Broeckhoven C
Hum Genet; 1997 Feb; 99(2):225-32. PubMed ID: 9048926
[TBL] [Abstract][Full Text] [Related]
13. Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.
Sato K; Yabe I; Fukuda Y; Soma H; Nakahara Y; Tsuji S; Sasaki H
Arch Neurol; 2010 Oct; 67(10):1257-62. PubMed ID: 20937954
[TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1.
Jöbsis GJ; Weber JW; Barth PG; Keizers H; Baas F; van Schooneveld MJ; van Hilten JJ; Troost D; Geesink HH; Bolhuis PA
J Neurol Neurosurg Psychiatry; 1997 Apr; 62(4):367-71. PubMed ID: 9120450
[TBL] [Abstract][Full Text] [Related]
15. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
Stevanin G; Bouslam N; Thobois S; Azzedine H; Ravaux L; Boland A; Schalling M; Broussolle E; Dürr A; Brice A
Ann Neurol; 2004 Jan; 55(1):97-104. PubMed ID: 14705117
[TBL] [Abstract][Full Text] [Related]
16. Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.
Verbeek DS; van de Warrenburg BP; Wesseling P; Pearson PL; Kremer HP; Sinke RJ
Brain; 2004 Nov; 127(Pt 11):2551-7. PubMed ID: 15306549
[TBL] [Abstract][Full Text] [Related]
17. North Carolina macular dystrophy phenotype in France maps to the MCDR1 locus.
Small KW; Puech B; Mullen L; Yelchits S
Mol Vis; 1997 Jan; 3():1. PubMed ID: 9238090
[TBL] [Abstract][Full Text] [Related]
18. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
Waters MF; Fee D; Figueroa KP; Nolte D; Müller U; Advincula J; Coon H; Evidente VG; Pulst SM
Neurology; 2005 Oct; 65(7):1111-3. PubMed ID: 16135769
[TBL] [Abstract][Full Text] [Related]
19. Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan.
Hayashi M; Adachi Y; Mori M; Nakano T; Nakashima K
Acta Neurol Scand; 2007 Aug; 116(2):123-7. PubMed ID: 17661799
[TBL] [Abstract][Full Text] [Related]
20. Autosomal dominant macular atrophy at 6q14 excludes CORD7 and MCDR1/PBCRA loci.
Griesinger IB; Sieving PA; Ayyagari R
Invest Ophthalmol Vis Sci; 2000 Jan; 41(1):248-55. PubMed ID: 10634627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
