Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Abnormalities and PINK1[original query] |
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Subclinical sensory abnormalities in unaffected PINK1 heterozygotes. Journal of neurology 2008 Sep 255 (9): 1372-7. Fiorio Mirta, Valente Enza Maria, Gambarin Mattia, Bentivoglio Anna Rita, Ialongo Tamara, Albanese Alberto, Barone Paolo, Pellecchia Maria Teresa, Brancati Francesco, Moretto Giuseppe, Fiaschi Antonio, Tinazzi Miche |
Screening PARK genes for mutations in early-onset Parkinson's disease patients from Queensland, Australia. Parkinsonism & related disorders 2009 Feb 15 (2): 105-9. Mellick George D, Siebert Gerhard A, Funayama Manabu, Buchanan Daniel D, Li Yuanzhe, Imamichi Yoko, Yoshino Hiroyo, Silburn Peter A, Hattori Nobuta |
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease. Journal of neurology, neurosurgery, and psychiatry 2010 Apr 81 (4): 391-5. Nishioka Kenya, Kefi Mounir, Jasinska-Myga Barbara, Wider Christian, Vilariño-Güell Carles, Ross Owen A, Heckman Michael G, Middleton Lefkos T, Ishihara-Paul Lianna, Gibson Rachel A, Amouri Rim, Ben Yahmed Samia, Ben Sassi Samia, Zouari Mourad, El Euch Ghada, Farrer Matthew J, Hentati Fayc |
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative cases. Parkinsonism & related disorders 2020 Aug 79 34-39. Tan Ai Huey, Lohmann Katja, Tay Yi Wen, Lim Jia Lun, Ahmad-Annuar Azlina, Ramli Norlisah, Chin Yen Theng, Mawardi Ahmad Shahir, Azmi Khairul, Aziz Zariah Abdul, Puvanarajah Santhi Datuk, Bauer Peter, Klein Christine, Rolfs Arndt, Lim Shen-Ya |
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