TY  - GEN
AU  - Waters,M F
AU  - Fee,D
AU  - Figueroa,K P
AU  - Nolte,D
AU  - Müller,U
AU  - Advincula,J
AU  - Coon,H
AU  - Evidente,V G
AU  - Pulst,S M
TI  - An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
SN  - 1526-632X
PY  - 2006///0309
KW  - Adult
KW  - Aged
KW  - Aged, 80 and over
KW  - Chromosome Disorders
KW  - genetics
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 19
KW  - DNA Mutational Analysis
KW  - Female
KW  - Genes, Dominant
KW  - Genetic Linkage
KW  - Genetic Predisposition to Disease
KW  - Genetic Testing
KW  - Genotype
KW  - Haplotypes
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - Pedigree
KW  - Penetrance
KW  - Phenotype
KW  - Philippines
KW  - Spinocerebellar Ataxias
N1  - 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
UR  - https://doi.org/10.1212/01.wnl.0000177490.05162.41
ER  -