Associated Papers
IMPACT OF ABCC8 AND TRPM4 GENETIC VARIATION IN CENTRAL NERVOUS SYSTEM DYSFUNCTION ASSOCIATED WITH PEDIATRIC SEPSIS.
Kernan KF et al.
Shock (augusta, Ga.), 2024
Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis.
Charfeddine C et al.
Plos One, 2021
34669720 (PubMed )
Supplement: pone.0258777.s002.xlsx › Feuil1
Select a paper to view details