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Novel SLC39A4 Mutation in Acrodermatitis Enteropathica

โœ Scribed by Alexandra Coromilas; Heather A. Brandling-Bennett; Kimberly D. Morel; Wendy K. Chung


Book ID
109091391
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
283 KB
Volume
28
Category
Article
ISSN
0736-8046

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An update on mutations of the SLC39A4 ge
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Acrodermatitis enteropathica (AE) is a very rare inherited recessive disease caused by severe zinc deficiency. It typically occurs in early infancy and is characterized by periorificial and acral dermatitis, alopecia, and diarrhea. In 2002, both we and others identified the AE SLC39A4 gene located a