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

Authors	Naohisa Ichiki, Chisato Tawada, Zenichiro Kato, Hajime Nakano, Mariko Seishima
Journal	The Journal of dermatology (J Dermatol) Vol. 48 Issue 12 Pg. e602-e603 (Dec 2021) ISSN: 1346-8138 [Electronic] England
PMID	34625996 (Publication Type: Letter)
Chemical References	Cation Transport Proteins Codon, Nonsense SLC39A4 protein, human Zinc
Topics	Acrodermatitis (diagnosis, genetics) Cation Transport Proteins (genetics) Codon, Nonsense Humans Japan Male Zinc (deficiency)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.

Realize the full power of the drug-disease research graph!