Associated Papers
Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature.
Zhong W et al.
Bmc Pediatrics, 2020
31987033 (PubMed )
Supplement: 12887_2020_1942_MOESM1_ESM.xlsx › Sheet1
Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle East.
Abu-Duhier F et al.
Dermatology Research and Practice, 2018
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
A new mutation in exon 3 of the SCL39A4 gene in a Tunisian family with severe acrodermatitis enteropathica.
Meftah SP et al.
Nutrition (burbank, Los Angeles County, Calif.), 2006
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