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Article

Omenn syndrome due to mutation of the RAG2 gene.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Dec 2009

Ktiouet S, Bertrand Y, Rival-Tringali A L, Kanitakis J, Malcus C, Poitevin F, Picard C, Claudy A, Faure M

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Source

Identifiers

PMID: 19470080
DOI: 10.1111/j.1468-3083.2009.03232.x

Genes

RAG2

Provenance

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Related research

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Research trail→

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Omenn syndrome due to mutation of the RAG2 gene.PMID 19470080Read ↗

A heterozygous mutation in the RAG2 gene with cutaneous and systemic manifestations partially resembling Omenn syndrome.Semantic proximity Read ↗

Omenn syndrome: a disorder of Rag1 and Rag2 genes.Semantic proximity Read ↗

Prenatal diagnosis of RAG-deficient Omenn syndrome.Semantic proximity Read ↗

[Analysis of genetic mutations and pathogenesis for two children with Omenn syndrome].Semantic proximity Read ↗

Omenn Syndrome and DNA recombination defects.Semantic proximity Read ↗

Whole-exome sequencing identified a homozygous novel RAG1 mutation in a child with omenn syndrome.Semantic proximity Read ↗

Diagnosing Omenn syndrome.Semantic proximity Read ↗

A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome.Semantic proximity Read ↗

RAG and RAG defects.Semantic proximity Read ↗

[Clinical phenotype and gene diagnostic analysis of Omenn syndrome].Semantic proximity Read ↗

Atypical Omenn Syndrome Due to RAG2 Gene Mutation, a Case Report.Semantic proximity Read ↗

First reported case of Omenn syndrome in a patient with reticular dysgenesis.Semantic proximity Read ↗

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