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Page 1
Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia.
Ben Halim N, Hsouna S, Lasram K, Rejeb I, Walha A, Talmoudi F, Messai H, Sabrine Ben Brick A, Ouragini H, Cherif W, Nagara M, Ben Rhouma F, Chouchene I, Ouechtati F, Bouyacoub Y, Ben Rekaya M, Messaoud O, Ben Ammar S, El Matri L, Tebib N, Ben Dridi MF, Mokni M, Amouri A, Kefi R, Abdelhak S. Ben Halim N, et al. Among authors: ouechtati f. Am J Hum Biol. 2016 Mar-Apr;28(2):171-80. doi: 10.1002/ajhb.22764. Epub 2015 Jul 16. Am J Hum Biol. 2016. PMID: 26179682
Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene.
Ouechtati F, Merdassi A, Bouyacoub Y, Largueche L, Derouiche K, Ouragini H, Nouira S, Tiab L, Baklouti K, Rebai A, Schorderet DF, Munier FL, Zografos L, Abdelhak S, El Matri L. Ouechtati F, et al. J Hum Genet. 2011 Jan;56(1):22-8. doi: 10.1038/jhg.2010.128. Epub 2010 Nov 25. J Hum Genet. 2011. PMID: 21107338
The metabolic signaling of the nucleoredoxin-like 2 gene supports brain function.
Jaillard C, Ouechtati F, Clérin E, Millet-Puel G, Corsi M, Aït-Ali N, Blond F, Chevy Q, Gales L, Farinelli M, Dalkara D, Sahel JA, Portais JC, Poncer JC, Léveillard T. Jaillard C, et al. Among authors: ouechtati f. Redox Biol. 2021 Nov 25;48:102198. doi: 10.1016/j.redox.2021.102198. Online ahead of print. Redox Biol. 2021. PMID: 34856436 Free PMC article.