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Mitochondrial dysfunction in Parkinson's disease.
Mizuno Y, Yoshino H, Ikebe S, Hattori N, Kobayashi T, Shimoda-Matsubayashi S, Matsumine H, Kondo T. Mizuno Y, et al. Among authors: hattori n. Ann Neurol. 1998 Sep;44(3 Suppl 1):S99-109. doi: 10.1002/ana.410440715. Ann Neurol. 1998. PMID: 9749580 Review.
Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.
Hattori N, Kitada T, Matsumine H, Asakawa S, Yamamura Y, Yoshino H, Kobayashi T, Yokochi M, Wang M, Yoritaka A, Kondo T, Kuzuhara S, Nakamura S, Shimizu N, Mizuno Y. Hattori N, et al. Ann Neurol. 1998 Dec;44(6):935-41. doi: 10.1002/ana.410440612. Ann Neurol. 1998. PMID: 9851438
2,489 results