Charfeddine, C., Laroussi, N., Mkaouar, R., Jouini, R., Khayat, O., Redissi, A., . . . Hammami-Ghorbel, H. (2021). Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis. Public Library of Science (PLoS).
Style de citation Chicago (17e éd.)Charfeddine, Cherine, et al. Expanding the Clinical Phenotype Associated with NIPAL4 Mutation: Study of a Tunisian Consanguineous Family with Erythrokeratodermia Variabilis-Like Autosomal Recessive Congenital Ichthyosis. Public Library of Science (PLoS), 2021.
Style de citation MLA (8e éd.)Charfeddine, Cherine, et al. Expanding the Clinical Phenotype Associated with NIPAL4 Mutation: Study of a Tunisian Consanguineous Family with Erythrokeratodermia Variabilis-Like Autosomal Recessive Congenital Ichthyosis. Public Library of Science (PLoS), 2021.