| 000 | 01566 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250513132641.0 | ||
| 264 | 0 | _c19980116 | |
| 008 | 199801s 0 0 eng d | ||
| 022 | _a0028-3878 | ||
| 024 | 7 |
_a10.1212/wnl.49.6.1598 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBandmann, O | |
| 245 | 0 | 0 |
_aMultiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration. _h[electronic resource] |
| 260 |
_bNeurology _cDec 1997 |
||
| 300 |
_a1598-604 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 | _aCiliary Neurotrophic Factor |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aInsulin-Like Growth Factor I _xmetabolism |
| 650 | 0 | 4 | _aMice |
| 650 | 0 | 4 |
_aMice, Neurologic Mutants _xgenetics |
| 650 | 0 | 4 |
_aMultiple System Atrophy _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aNerve Tissue Proteins _xgenetics |
| 650 | 0 | 4 |
_aReceptors, Somatomedin _xgenetics |
| 650 | 0 | 4 | _aRepetitive Sequences, Nucleic Acid |
| 650 | 0 | 4 | _aSequence Homology, Nucleic Acid |
| 650 | 0 | 4 |
_aSpinocerebellar Degenerations _xgenetics |
| 700 | 1 | _aSweeney, M G | |
| 700 | 1 | _aDaniel, S E | |
| 700 | 1 | _aWenning, G K | |
| 700 | 1 | _aQuinn, N | |
| 700 | 1 | _aMarsden, C D | |
| 700 | 1 | _aWood, N W | |
| 773 | 0 |
_tNeurology _gvol. 49 _gno. 6 _gp. 1598-604 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1212/wnl.49.6.1598 _zAvailable from publisher's website |
| 999 |
_c9378938 _d9378938 |
||