Zobrazeno 1 - 2
of 2
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
Autor:
Habibzadeh, Parham, Inaloo, Soroor, Silawi, Mohammad, Dastsooz, Hassan, Farazi Fard, Mohammad Ali, Sadeghipour, Forough, Faghihi, Zahra, Rezaeian, Mohaddeseh, Yavarian, Majid, Böhm, Johann, Faghihi, Mohammad Ali
Publikováno v:
Frontiers in Neurology; 9/4/2019, p1-6, 6p