SF
S. Fenniche

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
Téléchargements0