A novel SLC39A4 gene mutation in the family of an acrodermatitis enteropathica patient with an unusual presentation

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Bibliographic Details
Published inBritish journal of dermatology (1951) Vol. 159; no. 4; pp. 976 - 978
Main Authors Wang, S., Xue, L., Guo, Z-P., Wang, L., Yang, Y.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.10.2008
Blackwell
Subjects
Acrodermatitis - drug therapy
Acrodermatitis - genetics
Acrodermatitis - pathology
acrodermatitis enteropathica
Adult
Biological and medical sciences
Cation Transport Proteins - genetics
Dermatology
Female
Humans
Intestinal Absorption - genetics
Intestinal Absorption - physiology
Medical sciences
mutation
Mutation - genetics
Pedigree
Skin involvement in other diseases. Miscellaneous. General aspects
SLC39A4
Zinc - administration & dosage
Zinc - deficiency
Case study
Human
Skin disease
Gene
Dermatology
Family study
Digestive diseases
Mutation
Acrodermatitis enteropathica
Genetic disease
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Bibliography:istex:C445B8F48EF9089E283C6D432ABEF6F370B222C1
ark:/67375/WNG-TF18JRG0-L
ArticleID:BJD8777
Conflicts of interest: none declared.
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ISSN:0007-0963
1365-2133
DOI:10.1111/j.1365-2133.2008.08777.x