Charfeddine C, Laroussi N, Mkaouar R, Jouini R, et al. Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis. PLoS One 2021;16:e0258777.
PMID: 34669720