Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

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dc.contributor.authorLesage, Suzanne
dc.contributor.authorPatin, Etienne
dc.contributor.authorCondroyer, Christel
dc.contributor.authorLeutenegger, Anne-Louise
dc.contributor.authorLohmann, Ebba
dc.contributor.authorGiladi, Nir
dc.contributor.authorBar-Shira, Anat
dc.contributor.authorBelarbi, Soraya
dc.contributor.authorHecham, Nassima
dc.contributor.authorPollak, Pierre
dc.contributor.authorOuvrard-Hernandez, Anne-Marie
dc.contributor.authorBardien, Soraya
dc.contributor.authorCarr, Jonathan
dc.contributor.authorBenhassine, Traki
dc.contributor.authorTomiyama, Hiroyuki
dc.contributor.authorPirkevi, Caroline
dc.contributor.authorHamadouche, Tarik
dc.contributor.authorCazeneuve, Cécile
dc.contributor.authorBasak, A. Nazli
dc.contributor.authorHattori, Nobutaka
dc.contributor.authorDürr, Alexandra
dc.contributor.authorTazir, Meriem
dc.contributor.authorOrr-Urtreger, Avi
dc.contributor.authorQuintana-Murci, Lluis
dc.contributor.authorBrice, Alexis
dc.date.accessioned2015-06-24T10:43:12Z
dc.date.available2015-06-24T10:43:12Z
dc.date.issued2010
dc.identifier.issn09646906
dc.identifier.urihttps://dspace.univ-boumerdes.dz123456789/2075
dc.language.isoenen_US
dc.publisherOxford University Pressen_US
dc.relation.ispartofseriesHuman Molecular Genetics/ Vol.19, N°10 (2010);pp. 1998-2004
dc.subjectLRRK2en_US
dc.subjectG2019Sen_US
dc.subjectAutosomal Dominanten_US
dc.subjectParkinson's Disease (PD)en_US
dc.titleParkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humansen_US
dc.typeArticleen_US

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