| Literature DB >> 20300938 |
Cheng-Rang Li1, Shu-Mei Yan, Dan-Bei Shen, Qi Li, Jin-Ping Shao, Cheng-Yi Xue, Yuan-Hua Cao.
Abstract
Acrodermatitis enteropathica, a rare autosomal recessive disease, manifests as periorificial and symmetrical acral dermatitis, alopecia, and diarrhea due to insufficient zinc uptake by the intestine. Recent research revealed that mutations in the SLC39A4 gene are responsible for acrodermatitis enteropathica. This gene encodes one member of a human zinc transporter-like protein, also known as ZIP4. We detected one novel homozygous mutation c.1115T > G in the human SLC39A4 gene in one Chinese patient, which leading to p.L372R of the ZIP4. Homology analysis shows Leu372 in ZIP4 is conserved in Eutheria.Entities:
Mesh:
Substances:
Year: 2010 PMID: 20300938 DOI: 10.1007/s00403-010-1047-2
Source DB: PubMed Journal: Arch Dermatol Res ISSN: 0340-3696 Impact factor: 3.017