000 01329 a2200433 4500
005 20250513131328.0
264 0 _c19971208
008 199712s 0 0 eng d
022 _a0028-3878
024 7 _a10.1212/wnl.49.5.1247
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGeschwind, D H
245 0 0 _aSpinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations.
_h[electronic resource]
260 _bNeurology
_cNov 1997
300 _a1247-51 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAlleles
650 0 4 _aFamily Health
650 0 4 _aFemale
650 0 4 _aGene Frequency
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aSpinocerebellar Degenerations
_xdiagnosis
650 0 4 _aTrinucleotide Repeats
700 1 _aPerlman, S
700 1 _aFigueroa, K P
700 1 _aKarrim, J
700 1 _aBaloh, R W
700 1 _aPulst, S M
773 0 _tNeurology
_gvol. 49
_gno. 5
_gp. 1247-51
856 4 0 _uhttps://doi.org/10.1212/wnl.49.5.1247
_zAvailable from publisher's website
999 _c9341787
_d9341787