L. Largueche

Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene

Ahmed Rebai, D. Schorderet, S. Abdelhak, 2011, Journal of Human Genetics.

Optical Coherence Tomographic Findings in Berlin’s Edema

L. Largueche, L. el Matri, A. Chebil, 2010, Journal of ophthalmic & vision research.

Choroidal thickness measurement in highly myopic eyes using SD-OCT.

L. Largueche, L. el Matri, A. Chebil, 2012, Ophthalmic surgery, lasers & imaging : the official journal of the International Society for Imaging in the Eye.

Clinical Polymorphism of Stargardt Disease in a Large Consanguineous Tunisian Family; Implications for Nosology

S. Abdelhak, F. Ouechtati, L. Largueche, 2013, Journal of ophthalmic & vision research.

Contribution du SD-OCT de la macula dans le diagnostic de l’achromatopsie congénitale : à propos de 6 patients

L. Largueche, A. Chebil, L. Matri, 2014 .

Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients

C. Petit, J. Hardelin, S. Abdelhak, 2015, PloS one.

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

S. Abdelhak, F. Ouechtati, L. Largueche, 2013, Annales de biologie clinique.

Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene.

P. Söderkvist, L. Largueche, L. Matri, 2013, Gene.

A novel homozygous R764H mutation in crumbs homolog 1 causes autosomal recessive retinitis pigmentosa

D. Schorderet, F. Munier, L. Largueche, 2013, Molecular vision.

Epidemiologic study of myopia in a population of schoolchildren in Tunisia.

L. Largueche, L. el Matri, A. Chebil, 2016, La Tunisie medicale.

Identification of a novel mutation in FOXL2 gene that leads to blepharophimosis ptosis epicanthus inversus and telecanthus syndrome in a Tunisian consanguineous family.

S. Abdelhak, A. Amouri, L. Largueche, 2010, Genetic testing and molecular biomarkers.