000 01851 a2200589 4500
005 20250515073414.0
264 0 _c20080402
008 200804s 0 0 eng d
022 _a0340-6717
024 7 _a10.1007/s00439-007-0396-1
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHanein, Sylvain
245 0 0 _aA novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.
_h[electronic resource]
260 _bHuman genetics
_cNov 2007
300 _a261-73 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAge of Onset
650 0 4 _aAged
650 0 4 _aChild
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, Pair 10
_xgenetics
650 0 4 _aChromosomes, Human, Pair 8
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aGenetic Markers
650 0 4 _aHaplotypes
650 0 4 _aHumans
650 0 4 _aKinesins
_xgenetics
650 0 4 _aLod Score
650 0 4 _aMale
650 0 4 _aMicrosatellite Repeats
650 0 4 _aMiddle Aged
650 0 4 _aNerve Tissue Proteins
_xgenetics
650 0 4 _aNeuregulin-1
650 0 4 _aPedigree
650 0 4 _aSpastic Paraplegia, Hereditary
_xgenetics
700 1 _aDürr, Alexandra
700 1 _aRibai, Pascale
700 1 _aForlani, Sylvie
700 1 _aLeutenegger, Anne-Louise
700 1 _aNelson, Isabelle
700 1 _aBabron, Marie-Claude
700 1 _aElleuch, Nizar
700 1 _aDepienne, Christel
700 1 _aCharon, Céline
700 1 _aBrice, Alexis
700 1 _aStevanin, Giovanni
773 0 _tHuman genetics
_gvol. 122
_gno. 3-4
_gp. 261-73
856 4 0 _uhttps://doi.org/10.1007/s00439-007-0396-1
_zAvailable from publisher's website
999 _c17141354
_d17141354