Clinical utility gene card for: Acrodermatitis enteropathica

European Journal of Human Genetics

Volumn 20, Issue 3, 2012, Pages 365-

  Küry, Sébastien ^a   Kharfi, Monia ^b   Schmitt, Sébastien ^a   Bézieau, Stéphane ^a  

^a NANTES UNIVERSITY HOSPITAL   (France)

^b CHARLES NICOLLE HOSPITAL   (Tunisia)

Author keywords

[No Author keywords available]

Indexed keywords

ZINC; CATION TRANSPORT PROTEIN; SLC39A4 PROTEIN, HUMAN;

ACRODERMATITIS ENTEROPATHICA; ARTICLE; ATOPIC DERMATITIS; BIOINFORMATICS; CLINICAL FEATURE; CONTROLLED STUDY; DIAGNOSTIC TEST ACCURACY STUDY; DIFFERENTIAL DIAGNOSIS; ETHNIC GROUP; FRAMESHIFT MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HISTOPATHOLOGY; HUMAN; INCIDENCE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NONSENSE MUTATION; PREDICTIVE VALUE; PREVALENCE; PRIORITY JOURNAL; RISK FACTOR; SENSITIVITY AND SPECIFICITY; SINGLE NUCLEOTIDE POLYMORPHISM; SYMPTOM; ZINC DEFICIENCY; ACRODERMATITIS; GENETICS; MUTATION;

ACRODERMATITIS; CATION TRANSPORT PROTEINS; HUMANS; MUTATION; ZINC;

EID: 84857194199     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2011.227     Document Type: Article

References (13)

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