Crystallographic Modeling of the PNPT1:c.1453A>G Variant as a Cause of Mitochondrial Dysfunction and Autosomal Recessive Deafness; Expanding the Neuroimaging and Clinical Features

Publication date: Available online 1 April 2021Source: MitochondrionAuthor(s): Ali Hosseini Bereshneh, Zahra Rezaei, Ehsan Jafarinia, Fatemeh Rajabi, Mahmoud Reza Ashrafi, Ali Reza Tavasoli, Masoud Garshasbi
Source: Mitochondrion - Category: Biochemistry Source Type: research