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A new F-box protein 7 gene mutation causing typical Parkinson's disease

dc.contributor.authorGuven, Gamze
dc.contributor.authorHanagasi, Haşmet Ayhan
dc.contributor.authorEmre, Murat
dc.contributor.authorErginel-Unaltuna, Nihan
dc.contributor.authorGurvit, Hakan
dc.contributor.authorLEUTENEGGER, Anne L.
dc.contributor.authorDROUET, Valerie
dc.contributor.authorSAHBATOU, Mourad
dc.contributor.authorDELEUZE, Jean-Francois
dc.contributor.authorLESAGE, Suzanne
dc.contributor.authorBRICE, Alexis
dc.contributor.authorLohmann, Ebba
dc.contributor.authorCOQUEL, Anne-Sophie
dc.contributor.authorHONORE, Aurelie
dc.date.accessioned2021-03-03T15:50:35Z
dc.date.available2021-03-03T15:50:35Z
dc.date.issued2015
dc.identifier.citationLohmann E., COQUEL A., HONORE A., Gurvit H., Hanagasi H. A. , Emre M., LEUTENEGGER A. L. , DROUET V., SAHBATOU M., Guven G., et al., "A new F-box protein 7 gene mutation causing typical Parkinson's disease", MOVEMENT DISORDERS, cilt.30, sa.8, ss.1130-1133, 2015
dc.identifier.issn0885-3185
dc.identifier.othervv_1032021
dc.identifier.otherav_411c6cec-260a-4684-9a14-d4e395037a63
dc.identifier.urihttp://hdl.handle.net/20.500.12627/47502
dc.identifier.urihttps://doi.org/10.1002/mds.26266
dc.description.abstractBackgroundRecessive mutations in the F-box protein 7 gene (FBXO7; PARK15) have been identified as a cause of the parkinsonian-pyramidal syndrome. Here, we report clinical and genetic findings in a Turkish family with novel FBXO7 mutations.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleA new F-box protein 7 gene mutation causing typical Parkinson's disease
dc.typeMakale
dc.relation.journalMOVEMENT DISORDERS
dc.contributor.departmentInstitut National de la Sante et de la Recherche Medicale (Inserm) , ,
dc.identifier.volume30
dc.identifier.issue8
dc.identifier.startpage1130
dc.identifier.endpage1133
dc.contributor.firstauthorID28468


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