Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

Twinkal C. Pansuriya(Leiden University Medical Center), Ronald van Eijk(Leiden University Medical Center), Pio D’Adamo(University of Trieste), Maayke A.J.H. van Ruler(Leiden University Medical Center), Marieke L. Kuijjer(Leiden University Medical Center), Jan Oosting(Leiden University Medical Center), Anne‐Marie Cleton-Jansen(Leiden University Medical Center), Jolieke G. van Oosterwijk(Leiden University Medical Center), Sofie Verbeke(Leiden University Medical Center), Daniëlle Meijer(Leiden University Medical Center), Tom van Wezel(Leiden University Medical Center), Karolin H. Nord(Lund University), Luca Sangiorgi(Istituto Ortopedico Rizzoli), Berkin Toker(Istanbul University), Bernadette Liegl‐Atzwanger(Medical University of Graz), Mikel San-Julián(Clinica Universidad de Navarra), Raf Sciot(KU Leuven), Nisha Limaye(de Duve Institute), Lars‐Gunnar Kindblom(Royal Orthopaedic Hospital), Soeren Daugaard(University of Copenhagen), Catherine Godfraind(Cliniques Universitaires Saint-Luc), Laurence M. Boon(Cliniques Universitaires Saint-Luc), Miikka Vikkula(KU Leuven), Kyle C. Kurek(Harvard University), Károly Szuhai(Leiden University Medical Center), Pim J. French(Erasmus University Rotterdam), Judith V.M.G. Bovée(Leiden University Medical Center)
Nature Genetics
November 6, 2011
10.1038/ng.1004
Cited by 555Open Access
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