Recessive Parkinson's disease. |
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Authors: | Shin-ichiro Kubo Nobutaka Hattori Yoshikuni Mizuno |
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Affiliation: | Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan. |
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Abstract: | Parkinson's disease (PD) is a progressive neurodegenerative disease caused by loss of dopaminergic neurons in the substantia nigra pars compacta. Although the etiology of PD remains unclear, it is now clear that genetic factors contribute to the pathogenesis of the disease. Recently, several causative genes have been identified in monogenic forms of PD. Accumulating evidence indicates that their gene products play important roles in mitochondrial function, oxidative stress response, and the ubiquitin-proteasome system, which are also implicated in sporadic PD, suggesting that these gene products share a common pathway to nigral degeneration in both familial and sporadic PD. Here, we review recent advances in knowledge about genes associated with recessive PD, including parkin, PINK1, and DJ-1. |
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Keywords: | parkin PINK1 DJ‐1 recessive Parkinson's disease mitochondria oxidative stress ubiquitin–proteasome system |
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