One recurrent homozygous mutation ofSLC39A4in a girl with acrodermatitis enteropathica from southwestern China
Author:
Affiliation:
1. Institute of Dermatology and Venereology; Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital; Chengdu China
2. Department of Dermatology; West China Hospital; Sichuan University; Chengdu China
Funder
National Natural Science Foundation of China
Publisher
Wiley
Subject
Dermatology
Reference5 articles.
1. Acrodermatitis enteropathica: case report and review of literature;Perafán-Riveros;Pediatr Dermatol,2002
2. A novel SLC39A4 mutation in the family of an acrodermatitis enteropathica patient with an unusual presentation;Wang;Br J Dermatol,2008
3. An update on mutations of SLC39A4 gene in acrodermatitis enteropathica;Schmitt;Hum Mutat,2009
4. Mutation spectrum of human SLC39A4 in a panel of patients with acrodermatitis enteropathica;Küry;Hum Mutat,2003
5. A new mutation in exon 3 of SCL39A4 gene in a Tunisian family with severe acrodermatitis enteropathica;Meftah;Nutrition,2006
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1. Variants of SLC39A4 cause acrodermatitis enteropathica in Tibetan, Yi, and Han families in Sichuan region of southwestern China: a case report series;Frontiers in Medicine;2024-05-20
2. Novel nonsense mutation in the SLC39A4 gene in a Japanese boy with mild acrodermatitis enteropathica;The Journal of Dermatology;2021-10-08
3. Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature;BMC Pediatrics;2020-01-27
4. Acrodermatitis enteropathica: A novel mutation of theSLC39A4gene in a Turkish boy;The Journal of Dermatology;2016-02-24
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