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pro vyhledávání: '"Mohaddeseh Rezaeian"'
Autor:
Parham Habibzadeh, Soroor Inaloo, Mohammad Silawi, Hassan Dastsooz, Mohammad Ali Farazi Fard, Forough Sadeghipour, Zahra Faghihi, Mohaddeseh Rezaeian, Majid Yavarian, Johann Böhm, Mohammad Ali Faghihi
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Mitochondrial complex III deficiency nuclear type 2 is an autosomal-recessive disorder caused by mutations in TTC19 gene. TTC19 is involved in the preservation of mitochondrial complex III, which is responsible for transfer of electrons from reduced
Externí odkaz:
https://doaj.org/article/d312bc71ba574865a1c9b67a15653618
