Transient neonatal zinc deficiency in an infant
Author:
Affiliation:
1. Department of Dermatology University Hospitals Coventry and Warwickshire Coventry UK
Publisher
Wiley
Subject
Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ced.14755
Reference6 articles.
1. A novel homozygous mutation p.E88K in maternal SLC30A2 gene as a cause of transient neonatal zinc deficiency
2. Identification of a Mutation in SLC30A2 (ZnT-2) in Women with Low Milk Zinc Concentration That Results in Transient Neonatal Zinc Deficiency
3. Transient Neonatal Zinc Deficiency Due to a New Autosomal Dominant Mutation in GeneSLC30A2(ZnT-2)
4. Zinc deficiency and its management in the pediatric population: A literature review and proposed etiologic classification
5. Acrodermatitis enteropathica and an overview of zinc metabolism
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1. Novel SLC30A2 mutations in the pathogenesis of transient neonatal zinc deficiency;Pediatric Investigation;2023-02-22
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