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Possible Association of a Novel Missense Mutation A6375G in the Mitochondrial Cytochrome C Oxidase I Gene with Asthenospermia in the Tunisian Population

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


Book ID
115548901
Publisher
Mary Ann Liebert
Year
2012
Tongue
English
Weight
263 KB
Volume
16
Category
Article
ISSN
1945-0265

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m.6267G>A: a recurrent mutation in the h
✍ M. Esther Gallardo; Raquel Moreno-Loshuertos; Celia LΓ³pez; Mercedes Casqueiro; J πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 259 KB

Complete sequencing of the mitochondrial genome of 13 cell lines derived from a variety of human cancers revealed nine novel mitochondrial DNA (mtDNA) variations. One of them, m.6267G>A, is a recurrent mutation that introduces the Ala122Thr substitution in the mitochondrially encoded cytochrome c ox