Novel nonsense mutation in the SLC39A4 gene in a Japanese boy with mild acrodermatitis enteropathica

J Dermatol. 2021 Dec;48(12):e602-e603. doi: 10.1111/1346-8138.16184. Epub 2021 Oct 8.

Authors

Naohisa Ichiki¹, Chisato Tawada¹, Zenichiro Kato², Hajime Nakano³, Mariko Seishima¹

Affiliations

¹ Department of Dermatology, Gifu University Graduate School of Medicine, Gifu, Japan.
² Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu, Japan.
³ Department of Dermatology, Hirosaki University Graduate School of Medicine, Gifu, Japan.

PMID: 34625996
DOI: 10.1111/1346-8138.16184

No abstract available

Publication types

Letter

MeSH terms

Acrodermatitis* / diagnosis
Acrodermatitis* / genetics
Cation Transport Proteins* / genetics
Codon, Nonsense
Humans
Japan
Male
Zinc / deficiency

Substances

Cation Transport Proteins
Codon, Nonsense
SLC39A4 protein, human
Zinc

Supplementary concepts

Acrodermatitis enteropathica