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A Novel Member of a Zinc Transporter Family Is Defective in Acrodermatitis Enteropathica
The rare inherited condition acrodermatitis enteropathica (AE) results from a defect in the absorption of dietary zinc. Recently, we used homozygosity mapping in consanguineous Middle Eastern kindreds to localize the AE gene to an ∼3.5-cM region on 8q24. In this article, we identify a gene, SLC39A4,...
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| Publicado no: | Am J Hum Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2002
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC419995/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12032886/ https://ncbi.nlm.nih.govhttps://doi.org/10.1086/341125 |
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