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pro vyhledávání: '"Lamis El Harake"'
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Mitochondrial DNA depletion syndrome type 3 is an emerging disorder linked to variants in the deoxyguanosine kinase gene, which encodes for mitochondrial maintenance. This autosomal recessive disorder is frequent in the Middle East and
Externí odkaz:
https://doaj.org/article/a89c4c557b3b468aa080432dc66b03e6
