| 000 | 01554 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250515130658.0 | ||
| 264 | 0 | _c20080902 | |
| 008 | 200809s 0 0 eng d | ||
| 022 | _a1526-632X | ||
| 024 | 7 |
_a10.1212/01.wnl.0000320511.30222.dd _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aRoss, Owen A | |
| 245 | 0 | 0 |
_aCorticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations. _h[electronic resource] |
| 260 |
_bNeurology _cJul 2008 |
||
| 300 |
_a303; author reply 303-4 p. _bdigital |
||
| 500 | _aPublication Type: Letter; Comment | ||
| 650 | 0 | 4 |
_aAphasia, Primary Progressive _xgenetics |
| 650 | 0 | 4 | _aCausality |
| 650 | 0 | 4 |
_aDNA Mutational Analysis _xstandards |
| 650 | 0 | 4 |
_aGenetic Markers _xgenetics |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 |
_aGenetic Testing _xstandards |
| 650 | 0 | 4 |
_aGenetic Variation _xgenetics |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aInheritance Patterns _xgenetics |
| 650 | 0 | 4 | _aLeucine-Rich Repeat Serine-Threonine Protein Kinase-2 |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 |
_aNeurodegenerative Diseases _xgenetics |
| 650 | 0 | 4 | _aNorway |
| 650 | 0 | 4 |
_aParkinson Disease _xgenetics |
| 650 | 0 | 4 |
_aProtein Serine-Threonine Kinases _xgenetics |
| 650 | 0 | 4 | _aRisk Factors |
| 700 | 1 | _aToft, Mathias | |
| 700 | 1 | _aHaugarvoll, Kristoffer | |
| 773 | 0 |
_tNeurology _gvol. 71 _gno. 4 _gp. 303; author reply 303-4 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1212/01.wnl.0000320511.30222.dd _zAvailable from publisher's website |
| 999 |
_c18125066 _d18125066 |
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