Associated Papers
Classification of domains in predicted structures of the human proteome.
Schaeffer RD et al.
Proceedings of the National Academy of Sciences of the United States of America, 2023
36917664 (PubMed )
Supplement: pnas.2214069120.sd02.xlsx › Dataset_S2
A Missense Variant in SLC39A4 in a Litter of Turkish Van Cats with Acrodermatitis Enteropathica.
Kiener S et al.
Genes, 2021
Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle East.
Abu-Duhier F et al.
Dermatology Research and Practice, 2018
Crystal structures of a ZIP zinc transporter reveal a binuclear metal center in the transport pathway.
Zhang T et al.
Science Advances, 2017
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
An update on mutations of the SLC39A4 gene in acrodermatitis enteropathica.
Schmitt S et al.
Human Mutation, 2009
Regulation and function of Zip4, the acrodermatitis enteropathica gene.
Andrews GK
Biochemical Society Transactions, 2008
Acrodermatitis enteropathica mutations affect transport activity, localization and zinc-responsive trafficking of the mouse ZIP4 zinc transporter.
Wang F et al.
Human Molecular Genetics, 2004
Mutation spectrum of human SLC39A4 in a panel of patients with acrodermatitis enteropathica.
Küry S et al.
Human Mutation, 2003
The acrodermatitis enteropathica gene ZIP4 encodes a tissue-specific, zinc-regulated zinc transporter in mice.
Dufner-Beattie J et al.
The Journal of Biological Chemistry, 2003
Novel SLC39A4 mutations in acrodermatitis enteropathica.
Nakano A et al.
The Journal of Investigative Dermatology, 2003
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