Associated Papers
Transient Neonatal Zinc Deficiency Caused by a Novel Mutation in the SLC30A2 Gene.
Liew HM et al.
Pediatric Dermatology, 2017
Molecular Basis of Transient Neonatal Zinc Deficiency: NOVEL ZnT2 MUTATIONS DISRUPTING ZINC BINDING AND PERMEATION.
Golan Y et al.
The Journal of Biological Chemistry, 2016
Genetic causes and gene–nutrient interactions in mammalian zinc deficiencies: acrodermatitis enteropathica and transient neonatal zinc deficiency as examples.
Kasana S et al.
Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (gms), 2015
Transient neonatal zinc deficiency due to a new autosomal dominant mutation in gene SLC30A2 (ZnT-2).
Lova Navarro M et al.
Pediatric Dermatology, 0
Select a paper to view details