Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Settimini, L"'
Autor:
Settimini, L, Lenzi, Paola, Falleni, Alessandra, Valente, Em, Fornai, Francesco, Paparelli, Antonio
Mutations in the PTEN-induced putative kinase1 (PINK1) represent the second most common cause of autosomal recessive Parkinson’s disease. The PINK1 protein has a mitochondrial localization and interacts with a variety of proteins, including the pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df1152c064ff9e19e2df6d1c300cd513