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pro vyhledávání: '"Sebastian Kenvin"'
Autor:
Jeremi J Turkia, Jouni Kvist, Nadine Huber, Ras Trokovic, Vivek Sharma, Markus T. Sainio, Annakaisa Haapasalo, Jana Pennonen, Henna Tyynismaa, Emil Ylikallio, Sanna-Kaisa Herukka, Mari Auranen, Erika Rannila, Marco Reidelbach, Rubén Torregrosa-Muñumer, Sebastian Kenvin
Mutations in mitochondrial DNA encoded subunit of ATP synthase, MT-ATP6, are frequent causes of neurological mitochondrial diseases with a range of phenotypes from Leigh syndrome and NARP to ataxias and neuropathies. Here we investigated the function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2f50f541aa9661cc3bf7d89a952c14d
http://hdl.handle.net/10138/345126
http://hdl.handle.net/10138/345126
