HPCA confirmed as a genetic cause of DYT2‐like dystonia phenotype
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Published in Movement disorders (01.08.2018)
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Mutations in TYROBP are not a common cause of dementia in a Turkish cohort
Darwent, Lee, Carmona, Susana, Lohmann, Ebba, Guven, Gamze, Kun-Rodrigues, Celia, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Erginel-Unaltuna, Nihan, Pak, Meltem, Hardy, John, Singleton, Andrew, Brás, Jose, Guerreiro, Rita
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Published in Neurobiology of aging (01.10.2017)
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Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey
Kessler, Christoph, Atasu, Burcu, Hanagasi, Hasmet, Simón-Sánchez, Javier, Hauser, Ann-Kathrin, Pak, Meltem, Bilgic, Basar, Erginel-Unaltuna, Nihan, Gurvit, Hakan, Gasser, Thomas, Lohmann, Ebba
Published in Parkinsonism & related disorders (01.03.2018)
Published in Parkinsonism & related disorders (01.03.2018)
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