EVIDENCE FOR THE EXISTENCE OF A 4TH DOMINANTLY INHERITED SPINOCEREBELLAR ATAXIA LOCUS

被引:12
作者
LOPESCENDES, I
ANDERMANN, E
ROULEAU, GA
机构
[1] CTR RES NEUROSCI, MONTREAL, PQ, CANADA
[2] MONTREAL GEN HOSP, RES INST, MONTREAL H3G 1A4, PQ, CANADA
[3] MONTREAL NEUROL HOSP & INST, NEUROGENET UNIT, MONTREAL H3A 2B4, PQ, CANADA
[4] MCGILL UNIV, DEPT HUMAN GENET, MONTREAL, PQ, CANADA
[5] MCGILL UNIV, DEPT NEUROL & NEUROSURG, MONTREAL, PQ, CANADA
关键词
D O I
10.1006/geno.1994.1257
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The autosomal dominantly inherited spinocerebellar ataxias (SCAs) are a heterogeneous group of disorders. To date, three loci have been identified: the SCAI locus (on chr 6p), the SCA2 locus (on chr 12q), and more recently a Machado-Joseph disease (MJD) locus (on chr 14q). We have studied one large French-Canadian kindred with four generations of living affected individuals segregating an autosomal dominant form of SCk Linkage analysis using anonymous DNA markers that flank the three previously described loci significantly exclude the French-Canadian kindred from the SCAI, SCA2, and MJD loci, Therefore, a fourth, still unmapped SCA locus remains to be identified. In addition, the unique clinical phenotype present in all affected individuals of the French-Canadian kindred might be characteristic of this still unmapped SCA locus. (C) 1994 Academic Press, Inc.
引用
收藏
页码:270 / 274
页数:5
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