000 01219 a2200397 4500
005 20250513195059.0
264 0 _c19991130
008 199911s 0 0 eng d
022 _a0028-3878
024 7 _a10.1212/wnl.53.8.1844
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aReid, E
245 0 0 _aAutosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.
_h[electronic resource]
260 _bNeurology
_cNov 1999
300 _a1844-9 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, Pair 8
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aGenetic Variation
650 0 4 _aHumans
650 0 4 _aLod Score
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aParaplegia
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPhenotype
700 1 _aDearlove, A M
700 1 _aWhiteford, M L
700 1 _aRhodes, M
700 1 _aRubinsztein, D C
773 0 _tNeurology
_gvol. 53
_gno. 8
_gp. 1844-9
856 4 0 _uhttps://doi.org/10.1212/wnl.53.8.1844
_zAvailable from publisher's website
999 _c10519936
_d10519936