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Structure: Internal structure identifier : 410379

[Clinical characterization of the Stargardt disease and molecular exploration of the c.2041C>T mutation (ABCA4 gene) in Tunisian patients].

Ibtissem Chouchene , Leila Largueche , Farah Ouechtati , Kawthar Derouiche , Ahmed Turki , et al.
Annales de Biologie Clinique, 2013, 71 (6), pp.645-51. ⟨10.1684/abc.2013.0912⟩
Journal articles pasteur-01061094v1

Retinal dystrophy and congenital glaucoma as major causes of vision loss in students attending two institutions for the visually disabled in Tunis city, Tunisia.

I. Chouchene , K. Derouiche , N. Ben Halim , A. Merdassi , R. Limaiem , et al.
Journal Français d'Ophtalmologie, 2014, 37 (9), pp.695-701. ⟨10.1016/j.jfo.2014.03.010⟩
Journal articles pasteur-01375050v1
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Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.

Zied Riahi , Crystel Bonnet , Rim Zainine , Saida Lahbib , Yosra Bouyacoub , et al.
PLoS ONE, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
Journal articles pasteur-01221041v1
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Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia

Nizar Ben Halim , Sana Hsouna , Khaled Lasram , Insaf Rejeb , Asma Walha , et al.
American Journal of Human Biology, 2016, 28 (2), pp.171 - 180. ⟨10.1002/ajhb.22764⟩
Journal articles pasteur-01374977v1

Molecular detection and characterization through analysis of the hexon and fiber genes of Adenoviruses causing conjunctivitis in Tunisia, North Africa

Nadia Fedaoui , Narjess Ben Ayed , Ahlem Ben Yahia , Walid Hammami , Leila El Matri , et al.
Journal of Medical Virology, 2017, ⟨10.1002/jmv.24622⟩
Journal articles pasteur-01432788v1