000 01260 a2200397 4500
005 20250513125143.0
264 0 _c19980102
008 199801s 0 0 eng d
022 _a0964-6906
024 7 _a10.1093/hmg/6.11.1811
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aNielsen, J E
245 0 0 _aCAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.
_h[electronic resource]
260 _bHuman molecular genetics
_cOct 1997
300 _a1811-6 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aChromosomes, Human, Pair 2
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aGenetic Linkage
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aParaplegia
_xgenetics
650 0 4 _aPedigree
650 0 4 _aTrinucleotide Repeats
650 0 4 _aTumor Cells, Cultured
700 1 _aKoefoed, P
700 1 _aAbell, K
700 1 _aHasholt, L
700 1 _aEiberg, H
700 1 _aFenger, K
700 1 _aNiebuhr, E
700 1 _aSørensen, S A
773 0 _tHuman molecular genetics
_gvol. 6
_gno. 11
_gp. 1811-6
856 4 0 _uhttps://doi.org/10.1093/hmg/6.11.1811
_zAvailable from publisher's website
999 _c9280612
_d9280612