Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Rabih El Khoury"'
Autor:
Chen Yao, Rabih El Khoury, Wen Wang, Tara A. Byrd, Elizabeth A. Pehek, Colin Thacker, Xiongwei Zhu, Mark A. Smith, Amy L. Wilson-Delfosse, Shu G. Chen
Publikováno v:
Neurobiology of Disease, Vol 40, Iss 1, Pp 73-81 (2010)
Mutations in LRRK2 are thus far the most frequent known cause of autosomal dominant and idiopathic Parkinson's disease (PD) with prevalent mutations being found within the GTPase (R1441C/G) and kinase (G2019S) domains. Previous in vitro studies have
Externí odkaz:
https://doaj.org/article/973a9d85193c4136af315df55f2f93ea
Autor:
Elizabeth A. Pehek, Mark A. Smith, Chen Yao, Shu G. Chen, Wen Wang, Colin Thacker, Amy L. Wilson-Delfosse, Xiongwei Zhu, Rabih El Khoury, Tara A. Byrd
Publikováno v:
Neurobiology of Disease, Vol 40, Iss 1, Pp 73-81 (2010)
Mutations in LRRK2 are thus far the most frequent known cause of autosomal dominant and idiopathic Parkinson's disease (PD) with prevalent mutations being found within the GTPase (R1441C/G) and kinase (G2019S) domains. Previous in vitro studies have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebb25ab07e6551f84f8042e463525ade
https://europepmc.org/articles/PMC2926296/
https://europepmc.org/articles/PMC2926296/
