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Pseudo-heterozygous rearrangement mutation of parkin.
Funayama M, Yoshino H, Li Y, Kusaka H, Tomiyama H, Hattori N. Funayama M, et al. Among authors: li y. Mov Disord. 2012 Apr;27(4):552-5. doi: 10.1002/mds.24906. Epub 2012 Feb 5. Mov Disord. 2012. PMID: 22308057
Novel PINK1 mutations in early-onset parkinsonism.
Hatano Y, Li Y, Sato K, Asakawa S, Yamamura Y, Tomiyama H, Yoshino H, Asahina M, Kobayashi S, Hassin-Baer S, Lu CS, Ng AR, Rosales RL, Shimizu N, Toda T, Mizuno Y, Hattori N. Hatano Y, et al. Among authors: li y. Ann Neurol. 2004 Sep;56(3):424-7. doi: 10.1002/ana.20251. Ann Neurol. 2004. PMID: 15349870
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.
Tomiyama H, Li Y, Funayama M, Hasegawa K, Yoshino H, Kubo S, Sato K, Hattori T, Lu CS, Inzelberg R, Djaldetti R, Melamed E, Amouri R, Gouider-Khouja N, Hentati F, Hatano Y, Wang M, Imamichi Y, Mizoguchi K, Miyajima H, Obata F, Toda T, Farrer MJ, Mizuno Y, Hattori N. Tomiyama H, et al. Among authors: li y. Mov Disord. 2006 Aug;21(8):1102-8. doi: 10.1002/mds.20886. Mov Disord. 2006. PMID: 16622854
Progress in familial Parkinson's disease.
Mizuno Y, Hattori N, Yoshino H, Hatano Y, Satoh K, Tomiyama H, Li Y. Mizuno Y, et al. Among authors: li y. J Neural Transm Suppl. 2006;(70):191-204. doi: 10.1007/978-3-211-45295-0_30. J Neural Transm Suppl. 2006. PMID: 17017529 Review.
A new mutation in the GCH1 gene presents as early-onset Parkinsonism.
Momma K, Funayama M, Li Y, Ichinose H, Motoyoshi K, Hattori N, Mizuno Y, Kamakura K. Momma K, et al. Among authors: li y. Parkinsonism Relat Disord. 2009 Feb;15(2):160-1. doi: 10.1016/j.parkreldis.2007.12.010. Epub 2008 Jun 3. Parkinsonism Relat Disord. 2009. PMID: 18511327 No abstract available.
238,471 results
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