Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Locus heterogeneity in autosomal dominant spinocerebellar ataxia: Evidence for the existence of a fifth locus

Journal Article · · American Journal of Human Genetics
OSTI ID:134113
;  [1];  [2]
  1. Montreal General Hospital, Quebec (Canada)
  2. Montreal Neurological Institute and Hospital, Quebec (Canada); and others

The autosomal dominantly inherited spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerative disorders. To date, four loci have been identified: the SCA-1 locus (on chromosome (chr) 6p), the SCA-2 locus (on chr 12q), the SCA-3/MJD locus (on chr 14q), and more recently an SCA-4 locus was described (chr 16q) in a Utah kindred. We have studied one large French Canadian kindred with four generations of living affected individuals segregating an autosomal dominant form of SCA. Linkage analysis using anonymous DNA markers which flank the four previously described loci significantly excludes the French Canadian kindred from the SCA-1, SCA-2, SCA-3/MJD and SCA-4 loci. Therefore a fifth, still unmapped, SCA locus remains to be identified.

OSTI ID:
134113
Report Number(s):
CONF-941009--
Journal Information:
American Journal of Human Genetics, Journal Name: American Journal of Human Genetics Journal Issue: Suppl.3 Vol. 55; ISSN AJHGAG; ISSN 0002-9297
Country of Publication:
United States
Language:
English

Similar Records

Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locus
Journal Article · Sun May 01 00:00:00 EDT 1994 · Genomics; (United States) · OSTI ID:7029849

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region
Journal Article · Sun May 01 00:00:00 EDT 1994 · American Journal of Human Genetics; (United States) · OSTI ID:7160406

Genetic linkage studies in autosomal dominant ataxia families with an MJD phenotype
Journal Article · Thu Sep 01 00:00:00 EDT 1994 · American Journal of Human Genetics · OSTI ID:134723