000 01500 a2200433 4500
005 20250513090241.0
264 0 _c19960605
008 199606s 0 0 eng d
022 _a0001-6322
024 7 _a10.1007/BF00318569
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRobitaille, Y
245 0 0 _aStructural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype.
_h[electronic resource]
260 _bActa neuropathologica
_c1995
300 _a572-81 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAtrophy
650 0 4 _aBrain
_xpathology
650 0 4 _aChild
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, Pair 6
_xultrastructure
650 0 4 _aDentate Gyrus
_xpathology
650 0 4 _aHumans
650 0 4 _aImmunohistochemistry
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aNeural Pathways
_xpathology
650 0 4 _aOlivopontocerebellar Atrophies
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aRed Nucleus
_xpathology
650 0 4 _aSpinal Cord
_xpathology
650 0 4 _aSpinocerebellar Degenerations
_xgenetics
700 1 _aSchut, L
700 1 _aKish, S J
773 0 _tActa neuropathologica
_gvol. 90
_gno. 6
_gp. 572-81
856 4 0 _uhttps://doi.org/10.1007/BF00318569
_zAvailable from publisher's website
999 _c8614122
_d8614122