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

Author(s):
Pansuriya, T.C.; Eijk, R. van; d'Adamo, P.; Ruler, M.A.J.H. van; Kuijjer, M.L.; Oosting, J. (0000-0001-8894-1742); Cleton-Jansen, A.M.; Oosterwijk, J.G. van; Verbeke, S.L.J.; Meijer, D.; Wezel, T. van; Nord, K.H.; Sangiorgi, L.; Toker, B.; Liegl-Atzwanger, B.; San-Julian, M.; Sciot, R.; Limaye, N.; Kindblom, L.G.; Daugaard, S.; Godfraind, C.; Boon, L.M.; Vikkula, M.; Kurek, K.C.; Szuhai, K. (0000-0002-1228-4245); French, P.J.; Bovee, J.V.M.G. (0000-0003-1155-0481)
Published
2011
Publication type
Article / Letter to editor
Date issued
2011-12-31
Language
English
Is part of
Nature Genetics (2011), Vol. 43, no. 12, p. 1256-U124
hdl
1887/111411
doi
10.1038/ng.1004