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pro vyhledávání: '"Shouji Masanobu"'
Autor:
Imaizumi Yoichi, Okada Yohei, Akamatsu Wado, Koike Masato, Kuzumaki Naoko, Hayakawa Hideki, Nihira Tomoko, Kobayashi Tetsuro, Ohyama Manabu, Sato Shigeto, Takanashi Masashi, Funayama Manabu, Hirayama Akiyoshi, Soga Tomoyoshi, Hishiki Takako, Suematsu Makoto, Yagi Takuya, Ito Daisuke, Kosakai Arifumi, Hayashi Kozo, Shouji Masanobu, Nakanishi Atsushi, Suzuki Norihiro, Mizuno Yoshikuni, Mizushima Noboru, Amagai Masayuki, Uchiyama Yasuo, Mochizuki Hideki, Hattori Nobutaka, Okano Hideyuki
Publikováno v:
Molecular Brain, Vol 5, Iss 1, p 35 (2012)
Abstract Background Parkinson’s disease (PD) is a neurodegenerative disease characterized by selective degeneration of dopaminergic neurons in the substantia nigra (SN). The familial form of PD, PARK2, is caused by mutations in the parkin gene. par
Externí odkaz:
https://doaj.org/article/6d41288a5b94486dae4ca55aef26eb14