| 000 | 01706 a2200553 4500 | ||
|---|---|---|---|
| 005 | 20250514000639.0 | ||
| 264 | 0 | _c20010920 | |
| 008 | 200109s 0 0 eng d | ||
| 022 | _a1364-6745 | ||
| 024 | 7 |
_a10.1007/s100480000098 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAshley-Koch, A | |
| 245 | 0 | 0 |
_aFine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia. _h[electronic resource] |
| 260 |
_bNeurogenetics _cMar 2001 |
||
| 300 |
_a91-7 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 | _aChromosome Mapping |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 12 |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 19 |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 2 |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 8 |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes, Dominant |
| 650 | 0 | 4 | _aGenetic Linkage |
| 650 | 0 | 4 | _aGenetic Markers |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHaplotypes |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aLod Score |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aSpastic Paraplegia, Hereditary _xgenetics |
| 700 | 1 | _aBonner, E R | |
| 700 | 1 | _aGaskell, P C | |
| 700 | 1 | _aWest, S G | |
| 700 | 1 | _aTim, R | |
| 700 | 1 | _aWolpert, C M | |
| 700 | 1 | _aJones, R | |
| 700 | 1 | _aFarrell, C D | |
| 700 | 1 | _aNance, M | |
| 700 | 1 | _aSvenson, I K | |
| 700 | 1 | _aMarchuk, D A | |
| 700 | 1 | _aBoustany, R M | |
| 700 | 1 | _aVance, J M | |
| 700 | 1 | _aScott, W K | |
| 700 | 1 | _aPericak-Vance, M A | |
| 773 | 0 |
_tNeurogenetics _gvol. 3 _gno. 2 _gp. 91-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s100480000098 _zAvailable from publisher's website |
| 999 |
_c11287072 _d11287072 |
||