000 01769 a2200541 4500
005 20250515020527.0
264 0 _c20060425
008 200604s 0 0 eng d
022 _a0003-9942
024 7 _a10.1001/archneur.63.3.377
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGaig, Carles
245 0 0 _aLRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.
_h[electronic resource]
260 _bArchives of neurology
_cMar 2006
300 _a377-82 p.
_bdigital
500 _aPublication Type: Comparative Study; 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 _aAged, 80 and over
650 0 4 _aArginine
_xgenetics
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFamily Health
650 0 4 _aFemale
650 0 4 _aGene Frequency
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGlycine
_xgenetics
650 0 4 _aHumans
650 0 4 _aLeucine-Rich Repeat Serine-Threonine Protein Kinase-2
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aParkinson Disease
_xepidemiology
650 0 4 _aPedigree
650 0 4 _aProtein Serine-Threonine Kinases
_xgenetics
650 0 4 _aSerine
_xgenetics
650 0 4 _aSpain
_xepidemiology
700 1 _aEzquerra, Mario
700 1 _aMarti, Maria Jose
700 1 _aMuñoz, Esteban
700 1 _aValldeoriola, Francesc
700 1 _aTolosa, Eduardo
773 0 _tArchives of neurology
_gvol. 63
_gno. 3
_gp. 377-82
856 4 0 _uhttps://doi.org/10.1001/archneur.63.3.377
_zAvailable from publisher's website
999 _c16142931
_d16142931