1. 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. (25th April 2019) Authors: Sayeb, Marwa; Riahi, Zied; Laroussi, Nadia; Bonnet, Crystel; Romdhane, Lilia; Mkaouar, Rahma; Zaouak, Anissa; Marrakchi, Jihene; Abdessalem, Ghaith; Messaoud, Olfa; Bouchniba, Oussema; Ghilane, Nacer; Mokni, Mourad; Besbes, Ghazi; Yacoub‐Youssef, Houda; Petit, Christine; Abdelhak, Sonia Journal: International journal of dermatology Issue: Volume 58:Number 12(2019) Page Start: 1439 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗