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

Twinkal C. Pansuriya, Ronald van Eijk, Pio d'Adamo, Maayke A. J. H. van Ruler, Marieke L. Kuijjer, Jan Oosting, Anne-Marie Cleton-Jansen, Jolieke G. van Oosterwijk, Sofie L. J. Verbeke, Danielle Meijer, Tom van Wezel, Karolin Hansén Nord, Luca Sangiorgi, Berkin Toker, Bernadette Liegl-Atzwanger, Mikel San-Julian, Raf Sciot, Nisha Limaye, Lars-Gunnar Kindblom, Soeren DaugaardCatherine Godfraind, Laurence M. Boon, Miikka Vikkula, Kyle C. Kurek, Karoly Szuhai, Pim J. French, Judith V. M. G. Bovee

Research output: Contribution to journalArticlepeer-review

Fingerprint

Dive into the research topics of 'Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome'. Together they form a unique fingerprint.

Medicine & Life Sciences