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- The ZIP7 Gene (Slc39a7) Encodes a Zinc Transporter Involved in Zinc Homeostasis of the Golgi Apparatus
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- Фрактальный обнаружитель эхo-сигнала
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Zinc and Zinc Transporters in Dermatology
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