An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?

Waters, M F

An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus? [electronic resource] - Neurology Oct 2005 - 1111-3 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

1526-632X

10.1212/01.wnl.0000177490.05162.41 doi


Adult
Aged
Aged, 80 and over
Chromosome Disorders--genetics
Chromosome Mapping
Chromosomes, Human, Pair 19--genetics
DNA Mutational Analysis
Female
Genes, Dominant--genetics
Genetic Linkage--genetics
Genetic Predisposition to Disease--genetics
Genetic Testing
Genotype
Haplotypes
Humans
Male
Middle Aged
Mutation--genetics
Pedigree
Penetrance
Phenotype
Philippines
Spinocerebellar Ataxias--genetics