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Olfa Khayat

Publications (1)

Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis
Article scientifique · 2021

Domaines principaux

Sciences de la vie et biotechnologies1

Statistiques

Consultations2
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