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[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
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et al.
Journal articles
pasteur-01061094v1
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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 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.
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
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et al.
Journal articles
pasteur-01374977v1
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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 articles
pasteur-01432788v1
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