000 01807 a2200565 4500
005 20250515000722.0
264 0 _c20060309
008 200603s 0 0 eng d
022 _a1526-632X
024 7 _a10.1212/01.wnl.0000177490.05162.41
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWaters, M F
245 0 0 _aAn autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
_h[electronic resource]
260 _bNeurology
_cOct 2005
300 _a1111-3 p.
_bdigital
500 _aPublication 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.
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aAged, 80 and over
650 0 4 _aChromosome Disorders
_xgenetics
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, Pair 19
_xgenetics
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
_xgenetics
650 0 4 _aGenetic Linkage
_xgenetics
650 0 4 _aGenetic Predisposition to Disease
_xgenetics
650 0 4 _aGenetic Testing
650 0 4 _aGenotype
650 0 4 _aHaplotypes
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPenetrance
650 0 4 _aPhenotype
650 0 4 _aPhilippines
650 0 4 _aSpinocerebellar Ataxias
_xgenetics
700 1 _aFee, D
700 1 _aFigueroa, K P
700 1 _aNolte, D
700 1 _aMüller, U
700 1 _aAdvincula, J
700 1 _aCoon, H
700 1 _aEvidente, V G
700 1 _aPulst, S M
773 0 _tNeurology
_gvol. 65
_gno. 7
_gp. 1111-3
856 4 0 _uhttps://doi.org/10.1212/01.wnl.0000177490.05162.41
_zAvailable from publisher's website
999 _c15771703
_d15771703