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Article

Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2

6 Nov 2011

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22057236
DOI: 10.1038/ng.994

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2PMID 22057236Read ↗

Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndromeSemantic proximity Read ↗

Gene of the month: IDH1.Semantic proximity Read ↗

An intermediate phenotype in IDH related enchondromatosis spectrum.Semantic proximity Read ↗

IDH1 R132C and ERC2 L309I Mutations Contribute to the Development of Maffucci's Syndrome.Semantic proximity Read ↗

Somatic IDH1 variant (p.R132C) in an adult male with Maffucci syndrome.Semantic proximity Read ↗

Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndromeSemantic proximity Read ↗

Rare IDH1 variants are common in pediatric hemispheric diffuse astrocytomas and frequently associated with Li-Fraumeni syndrome.Semantic proximity Read ↗

IDH1 and IDH2: Not Your Typical OncogenesSemantic proximity Read ↗

Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia.Semantic proximity Read ↗

Aicardi-Goutières Syndrome Is Caused by IFIH1 MutationsSemantic proximity Read ↗

Emerging bone marrow failure syndromes- new pieces to an unsolved puzzleSemantic proximity Read ↗

Genetic characterization of acute myeloid leukemia patients with mutations in IDH1/2 genes.Semantic proximity Read ↗

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