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A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co-occurrence of hearing loss in a child due to mutation in the SLC26A4 gene |
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| Authors: | Marwa Sayeb PhD Zied Riahi PhD Nadia Laroussi PhD Crystel Bonnet PhD Lilia Romdhane PhD Rahma Mkaouar PhD Anissa Zaouak MD Jihene Marrakchi MD Ghaith Abdessalem PhD Olfa Messaoud PhD Oussema Bouchniba MS Nacer Ghilane MS Mourad Mokni MD Ghazi Besbes MD Houda Yacoub-Youssef PhD Christine Petit MD PhD Sonia Abdelhak PhD |
| Affiliation: | 1. Laboratory of Biomedical Genomics and Oncogenetics (LR11IPT05), University of Tunis El Manar, Pasteur Institut of Tunis, Tunis, Tunisia;2. Laboratory of Biomedical Genomics and Oncogenetics (LR11IPT05), University of Tunis El Manar, Pasteur Institut of Tunis, Tunis, Tunisia INSERM, UMRS 1120, Vision Institut, Paris, France University of Paris VI UPMC Sorbonnes, Paris, France;3. INSERM, UMRS 1120, Vision Institut, Paris, France University of Paris VI UPMC Sorbonnes, Paris, France;4. Laboratory of Biomedical Genomics and Oncogenetics (LR11IPT05), University of Tunis El Manar, Pasteur Institut of Tunis, Tunis, Tunisia Department of Biology, Faculty of Science of Bizerte, Université Tunis Carthage, Zarzouna, Tunisia;5. Department of Dermatology, Habib Thameur Hospital, Tunis, Tunisia;6. Department of Otorhinolaryngology, CHU La Rabta, Tunis, Tunisia;7. Departement of Biochemistry, Habib Bourguiba Hospital, Medenine, Tunisia;8. Department of Dermatology, CHU La Rabta Tunis, Tunis, Tunisia;9. INSERM, UMRS 1120, Vision Institut, Paris, France University of Paris VI UPMC Sorbonnes, Paris, France Unité de Génétique et Physiologie de l'Audition, Institut Pasteur, Paris, France Collège de France, Paris, France |
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