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 |