A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene-Reference-Cited by-同舟云学术

A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene

Published:2019-04-25 Issue:12 Volume:58 Page:1439-1443
ISSN:0011-9059
Container-title:International Journal of Dermatology
language:en
Short-container-title:Int J Dermatol

Author:

Sayeb Marwa¹,Riahi Zied¹²³,Laroussi Nadia¹,Bonnet Crystel²³,Romdhane Lilia¹⁴,Mkaouar Rahma¹,Zaouak Anissa⁵^ORCID,Marrakchi Jihene⁶,Abdessalem Ghaith¹,Messaoud Olfa¹,Bouchniba Oussema⁷,Ghilane Nacer⁷,Mokni Mourad⁸,Besbes Ghazi⁶,Yacoub‐Youssef Houda¹,Petit Christine²³⁹¹⁰,Abdelhak Sonia¹

Affiliation:

1. Laboratory of Biomedical Genomics and Oncogenetics (LR11IPT05) University of Tunis El Manar Pasteur Institut of Tunis Tunis Tunisia

2. INSERM UMRS 1120 Vision Institut Paris France

3. University of Paris VI UPMC Sorbonnes Paris France

4. Department of Biology Faculty of Science of Bizerte Université Tunis Carthage ZarzounaTunisia

5. Department of Dermatology Habib Thameur Hospital TunisTunisia

6. Department of Otorhinolaryngology CHU La Rabta TunisTunisia

7. Departement of Biochemistry Habib Bourguiba Hospital MedenineTunisia

8. Department of Dermatology CHU La Rabta Tunis Tunis Tunisia

9. Unité de Génétique et Physiologie de l'Audition Institut Pasteur Paris France

10. Collège de France Paris France

Funder