Zobrazeno 1 - 2
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pro vyhledávání: '"Bowles Erin E"'
Autor:
Hinkle Kelly M, Yue Mei, Behrouz Bahareh, Dächsel Justus C, Lincoln Sarah J, Bowles Erin E, Beevers Joel E, Dugger Brittany, Winner Beate, Prots Iryna, Kent Caroline B, Nishioka Kenya, Lin Wen-Lang, Dickson Dennis W, Janus Christopher J, Farrer Matthew J, Melrose Heather L
Publikováno v:
Molecular Neurodegeneration, Vol 7, Iss 1, p 25 (2012)
Abstract Mutations in the LRRK2 gene are the most common cause of genetic Parkinson’s disease. Although the mechanisms behind the pathogenic effects of LRRK2 mutations are still not clear, data emerging from in vitro and in vivo models suggests rol
Externí odkaz:
https://doaj.org/article/6c25dd1f24ef43c6948b6a69831ef927
Autor:
Hinkle, Kelly M, Yue, Mei, Behrouz, Bahareh, Dachsel, Justus C, Lincoln, Sarah J, Bowles, Erin E, Beevers, Joel E, Dugger, Brittany, Winner, Beate, Prots, Iryna, Kent, Caroline B, Nishioka, Kenya, Wen-Lang Lin, Janus, Christopher, Dickson, Dennis W, Farrer, Matthew J, Melrose, Heather L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbc635db60fdcf0778e436934d031aa9
