| 000 | 01508 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250515052759.0 | ||
| 264 | 0 | _c20080123 | |
| 008 | 200801s 0 0 eng d | ||
| 022 | _a1364-6745 | ||
| 024 | 7 |
_a10.1007/s10048-006-0074-9 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKlebe, Stephan | |
| 245 | 0 | 0 |
_aNIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe. _h[electronic resource] |
| 260 |
_bNeurogenetics _cApr 2007 |
||
| 300 |
_a155-7 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAge of Onset |
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aEurope |
| 650 | 0 | 4 | _aExons |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes, Dominant |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMembrane Proteins _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aParaplegia _xgenetics |
| 700 | 1 | _aLacour, Arnaud | |
| 700 | 1 | _aDurr, Alexandra | |
| 700 | 1 | _aStojkovic, Tanya | |
| 700 | 1 | _aDepienne, Christel | |
| 700 | 1 | _aForlani, Sylvie | |
| 700 | 1 | _aPoea-Guyon, Sandrine | |
| 700 | 1 | _aVuillaume, Isabelle | |
| 700 | 1 | _aSablonniere, Bernard | |
| 700 | 1 | _aVermersch, Patrick | |
| 700 | 1 | _aBrice, Alexis | |
| 700 | 1 | _aStevanin, Giovanni | |
| 773 | 0 |
_tNeurogenetics _gvol. 8 _gno. 2 _gp. 155-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s10048-006-0074-9 _zAvailable from publisher's website |
| 999 |
_c16771488 _d16771488 |
||