Possible association of a novel missense mutation A6375G in the mitochondrial cytochrome C oxidase I gene with asthenospermia in the Tunisian population

Siwar Baklouti-Gargouri, Myriam Ghorbel, Imen Chamkha, Emna Mkaouar-Rebai, Afifa Sellami, Nozha Chakroun, Faiza Fakhfakh, Leila Ammar-Keskes

Research output: Contribution to journal › Article › peer-review

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Medicine & Life Sciences