Zobrazeno 1 - 1
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pro vyhledávání: '"and acad9 genes"'
Autor:
E. A. Nikolaeva
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 60, Iss 3, Pp 21-25 (2016)
The common cause of mitochondrial diseases is hereditary defects in mitochondrial respiratory chain complex I, which account for about 30% of the cases of mitochondrial diseases in children. Complex I is the largest and most complicated enzyme comple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::756e98ad5c3c84290af0f5c6a5c3e04d
https://www.ped-perinatology.ru/jour/article/view/186
https://www.ped-perinatology.ru/jour/article/view/186
