Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice von Nair, K Saidas, Hmani-Aifa, Mounira, Ali, Zain, Kearney, Alison L, Salem, Salma Ben, Macalinao, Danilo G, Cosma, Ioan M, Bouassida, Walid, Hakim, Bochra, Benzina, Zeineb, Soto, Ileana, Söderkvist, Peter, Howell, Gareth R, Smith, Richard S, Ayadi, Hammadi, John, Simon W M

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Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family von HMANI-AIFA, Mounira, BENZINA, Zeineb, AYADI, Hammadi, ZULFIQAR, Fareeha, DHOUIB, Houria, SHAHZADI, Amber, GHORBEL, Abdelmonem, REBAI, Ahmed, SÖDERKVIST, Peter, RIAZUDDIN, Sheikh, KIMBERLING, William J

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The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene von Ayadi, Hammadi, Lévy, Gallia, Weil, Dominique, Levi-Acobas, Fabienne, Drira, Mohamed, Blanchard, Stéphane, Petit, Christine, Küssel, Polonca

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Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness von Ben Arab, Saida, Masmoudi, Saber, Beltaief, Najeh, Hachicha, Slah, Ayadi, Hammadi

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The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population von Chabchoub, Ghazi, Teixiera, Elisabeth Petit, Maalej, Abdellatif, Hamad, Mariem Ben, Bahloul, Zouheir, Cornelis, Francois, Ayadi, Hammadi

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Cloning and Characterization of SLC26A6, a Novel Member of the Solute Carrier 26 Gene Family von Waldegger, Siegfried, Moschen, Ivano, Ramirez, Alfredo, Smith, Richard J.H., Ayadi, Hammadi, Lang, Florian, Kubisch, Christian

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PDS Is a New Susceptibility Gene to Autoimmune Thyroid Diseases: Association and Linkage Study von Kacem, Hassen Hadj, Rebai, Ahmed, Kaffel, Noureddine, Masmoudi, Saber, Abid, Mohamed, Ayadi, Hammadi

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Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations von Bouchlaka, Chiraz, Abdelhak, Sonia, Amouri, Ahlem, Ben Abid, Hela, Hadiji, Sondes, Frikha, Mounir, Ben Othman, Tarek, Amri, Fethi, Ayadi, Hammadi, Hachicha, Mongia, Rebaï, Ahmed, Saad, Ali, Dellagi, Koussay

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Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis von Ben-Rebeh, Imen, Grati, Mhamed, Bonnet, Crystel, Bouassida, Walid, Hadjamor, Imen, Ayadi, Hammadi, Ghorbel, Abdelmonem, Petit, Christine, Masmoudi, Saber

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Retracted : Genotyping of Tunisian azoospermic men with Sertoli cell-only and maturation arrest: Genotyping of SCO and maturation arrest patients von Hadjkacem-Loukil, Lobna, Hadj-kacem, Hassen, Hadj Salem, Ikhlass, Bahloul, Ali, Fakhfakh, Faiza, Ayadi, Hammadi

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IL-1β and TSH disturb thyroid epithelium integrity in autoimmune thyroid diseases von Rebuffat, Sandra A, Kammoun-Krichen, Maha, Charfeddine, Ilhem, Ayadi, Hammadi, Bougacha-Elleuch, Noura, Peraldi-Roux, Sylvie

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Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases von Chabchoub, Ghazi, Uz, Elif, Maalej, Abdellatif, Mustafa, Chigdem A, Rebai, Ahmed, Mnif, Mouna, Bahloul, Zouheir, Farid, Nadir R, Ozcelik, Tayfun, Ayadi, Hammadi

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Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin von Weil, Dominique, El-Amraoui, Aziz, Masmoudi, Saber, Mustapha, Mirna, Kikkawa, Yoshiaki, Lainé, Sophie, Delmaghani, Sedigheh, Adato, Avital, Nadifi, Sellama, Zina, Zeineb Ben, Hamel, Christian, Gal, Andreas, Ayadi, Hammadi, Yonekawa, Hiromichi, Petit, Christine

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Potential Predictive Role of Lipid Peroxidation Markers for Type 2 Diabetes in the Adult Tunisian Population von Bouhajja, Houda, Kacem, Faten Hadj, Abdelhedi, Rania, Ncir, Marwa, Dimitrov, Jordan D., Marrakchi, Rim, Jamoussi, Kamel, Rebai, Ahmed, El Feki, Abdelfattah, Abid, Mohamed, Ayadi, Hammadi, Kaveri, Srini V., Mnif-Feki, Mouna, Bougacha-Elleuch, Noura

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Proteomic approaches for discovering biomarkers of diabetic nephropathy von Ben Ameur, Randa, Molina, Laurence, Bolvin, Capucine, Kifagi, Chamseddine, Jarraya, Fayçal, Ayadi, Hammadi, Molina, Franck, Granier, Claude

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Affinity kinetics of leptin-reactive immunoglobulins are associated with plasma leptin and markers of obesity and diabetes von Bouhajja, Houda, Bougacha-Elleuch, Noura, Lucas, Nicolas, Legrand, Romain, Marrakchi, Rim, Kaveri, Srini V., Jamoussi, Kamel, Ayadi, Hammadi, Abid, Mohamed, Mnif-Feki, Mouna, Fetissov, Sergueï O.

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Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene von Said, Mariem Ben, Chouchène, Ebtissem, Salem, Salma Ben, Daoud, Kods, Largueche, Leila, Bouassida, Walid, Benzina, Zeineb, Ayadi, Hammadi, Söderkvist, Peter, Matri, Leila, Hmani-Aifa, Mounira

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Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect von Bougacha-Elleuch, Noura, Charfi, Nadia, Miled, Nabil, Bouhajja, Houda, Belguith, Neila, Mnif, Mouna, Jaurge, Paula, Chikhrouhou, Nessrine, Ayadi, Hammadi, Hachicha, Mongia, Abid, Mohamed

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Retracted: Genotyping of Tunisian azoospermic men with Sertoli cell‐only and maturation arrest von Hadjkacem‐Loukil, Lobna, Hadj‐kacem, Hassen, Hadj Salem, Ikhlass, Bahloul, Ali, Fakhfakh, Faiza, Ayadi, Hammadi

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Erratum to: Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect von Bougacha-Elleuch, Noura, Charfi, Nadia, Miled, Nabil, Bouhajja, Houda, Belguith, Neila, Mnif, Mouna, Jorge, Paula, Chikhrouhou, Nessrine, Ayadi, Hammadi, Hachicha, Mongia, Abid, Mohamed

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