Zinc transporter mutations linked to acrodermatitis enteropathica disrupt function and cause mistrafficking

ZIP4 is a representative member of the Zrt-/Irt-like protein (ZIP) transporter family and responsible for zinc uptake from diet. Loss-of-function mutations of human ZIP4 (hZIP4) drastically reduce zinc absorption, causing a life-threatening autosomal recessive disorder, acrodermatitis enteropathica...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:J Biol Chem
Asıl Yazarlar: Kuliyev, Eziz, Zhang, Chi, Sui, Dexin, Hu, Jian
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Biochemistry and Molecular Biology 2021
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7949036/
https://ncbi.nlm.nih.gov/pubmed/33837739
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jbc.2021.100269
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