Novel nonsense mutation in the SLC39A4 gene in a Japanese boy with mild acrodermatitis enteropathica-Reference-Cited by-同舟云学术

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

Published:2021-10-08 Issue:12 Volume:48 Page:
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J. Dermatol.

Author:

Ichiki Naohisa¹^ORCID,Tawada Chisato¹,Kato Zenichiro²,Nakano Hajime³,Seishima Mariko¹

Affiliation:

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

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.16184

Reference5 articles.

1. 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

2. Novel SLC39A4 Mutations in Acrodermatitis Enteropathica

3. Mutation spectrum of humanSLC39A4in a panel of patients with acrodermatitis enteropathica

4. A new mutation in exon 3 of the SCL39A4 gene in a Tunisian family with severe acrodermatitis enteropathica

5. One recurrent homozygous mutation ofSLC39A4in a girl with acrodermatitis enteropathica from southwestern China

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1. Acquired and Inherited Zinc Deficiency-Related Diseases in Children: A Case Series and a Narrative Review;Pediatric Reports;2024-07-25

2. Diet management in congenital diarrheas and enteropathies – general concepts and disease-specific approach, a narrative review;The American Journal of Clinical Nutrition;2024-07

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