000 01628 a2200517 4500
005 20250514164547.0
264 0 _c20040203
008 200402s 0 0 eng d
022 _a1526-632X
024 7 _a10.1212/01.wnl.0000098883.79421.73
_2doi
040 _aNLM
_beng
_cNLM
100 1 _avan de Warrenburg, B P C
245 0 0 _aIdentification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family.
_h[electronic resource]
260 _bNeurology
_cDec 2003
300 _a1760-5 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aAge of Onset
650 0 4 _aAged
650 0 4 _aAged, 80 and over
650 0 4 _aCerebellar Ataxia
_xdiagnosis
650 0 4 _aChromosomes, Human, Pair 19
_xgenetics
650 0 4 _aDNA Mutational Analysis
650 0 4 _aExons
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aGenetic Linkage
650 0 4 _aHaplotypes
650 0 4 _aHumans
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation, Missense
650 0 4 _aNetherlands
_xepidemiology
650 0 4 _aPedigree
650 0 4 _aProtein Kinase C
_xgenetics
700 1 _aVerbeek, D S
700 1 _aPiersma, S J
700 1 _aHennekam, F A M
700 1 _aPearson, P L
700 1 _aKnoers, N V A M
700 1 _aKremer, H P H
700 1 _aSinke, R J
773 0 _tNeurology
_gvol. 61
_gno. 12
_gp. 1760-5
856 4 0 _uhttps://doi.org/10.1212/01.wnl.0000098883.79421.73
_zAvailable from publisher's website
999 _c14424875
_d14424875