Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23–q24.1
- 20 January 1995
- Vol. 25 (2), 433-435
- https://doi.org/10.1016/0888-7543(95)80043-l
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Evidence for the Existence of a Fourth Dominantly Inherited Spinocerebellar Ataxia LocusGenomics, 1994
- Integrated human genome–wide maps constructed using the CEPH reference panelNature Genetics, 1994
- Anticipation in spinocerebellar ataxia type 2Nature Genetics, 1993
- Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1Nature Genetics, 1993
- Search for the Chromosomal Location of Autosomal Dominant Cerebellar Ataxia from Holguin, Cuba: Exclusion from Candidate Regions on Chromosome 4 and 11qHuman Heredity, 1993
- Report of the committee on the genetic constitution of chromosome 12Cytogenetic and Genome Research, 1991
- PCR detection of the Mspl (Aa) RFLP at the human phenylalanine hydroxylase (PAH) locusNucleic Acids Research, 1991
- Autosomal dominant cerebellar ataxiaNeurology, 1990
- CLASSIFICATION OF THE HEREDITARY ATAXIAS AND PARAPLEGIASThe Lancet, 1983
- HEREDITARY ATAXIAArchives of Neurology & Psychiatry, 1950