Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis.

Autor:	Charfeddine, Cherine1,2 (AUTHOR) cherine.charfeddine@gmail.com, Laroussi, Nadia1 (AUTHOR), Mkaouar, Rahma1 (AUTHOR), Jouini, Raja3 (AUTHOR), Khayat, Olfa3 (AUTHOR), Redissi, Aladin4 (AUTHOR), Mosbah, Amor4 (AUTHOR), Dallali, Hamza1 (AUTHOR), Chedly Debbiche, Achraf3 (AUTHOR), Zaouak, Anissa5 (AUTHOR), Fenniche, Sami5 (AUTHOR), Abdelhak, Sonia1 (AUTHOR), Hammami-Ghorbel, Houda5 (AUTHOR)
Zdroj:	PLoS ONE. 10/20/2021, Vol. 16 Issue 10, p1-21. 21p.
Databáze:	Academic Search Ultimate
Externí odkaz:	Zobrazit plný text záznamu