A new genetic isolate of acrodermatitis enteropathica with a novel mutation
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2009.09128.x/fullpdf
Reference10 articles.
1. Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3;Wang;Am J Hum Genet,2001
2. Identification of SLC39A4, a gene involved in acrodermatitis enteropathica;Kury;Nat Genet,2002
3. A novel member of a zinc transporter family is defective in acrodermatitis enteropathica;Wang;Am J Hum Genet,2000
4. Acrodermatitis enteropathica mutations affect transport activity, localization and zinc-responsive trafficking of the mouse ZIP4 zinc transporter;Wang;Hum Mol Genet,2004
5. Mutation spectrum of human SLC39A4 in a panel of patients with acrodermatitis enteropathica;Kury;Hum Mutat,2003
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1. A 14-month-old girl diagnosed with acrodermatitis enteropathica with SLC39A4 gene mutation;Revue Française d'Allergologie;2022-12
2. Genetic causes and gene–nutrient interactions in mammalian zinc deficiencies: Acrodermatitis enteropathica and transient neonatal zinc deficiency as examples;Journal of Trace Elements in Medicine and Biology;2015-01
3. Acrodermatitis enteropática: caso clínico y revisión de la literatura;Revista médica de Chile;2013-11
4. Variations in Solute Transporter Genes Affecting Micronutrient Solute Transport and Human Health;Nutrigenomics and Nutrigenetics in Functional Foods and Personalized Nutrition;2013-07-25
5. Degenerative and metabolic diseases;McKee's Pathology of the Skin;2012
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