• Mutation; HGNC; HGNC:5382; IDH1; None_reported; -; Zygosity=- (PubMed=22057234).
  
• Mutation; HGNC; HGNC:5383; IDH2; None_reported; -; Zygosity=- (PubMed=22057234).
  
• Mutation; HGNC; HGNC:11998; TP53; None_reported; -; Zygosity=- (PubMed=15731924).
  

PubMed=15731924; DOI=10.1007/s00428-004-1194-y
Kalinski T., Krueger S., Pelz A.-F., Wieacker P.F., Hartig R., Ropke M., Schneider-Stock R., Dombrowski F., Roessner A.
Establishment and characterization of the permanent human cell line C3842 derived from a secondary chondrosarcoma in Ollier's disease.
Virchows Arch. 446:287-299(2005)

PubMed=22057234; DOI=10.1038/ng.1004; PMCID=PMC3427908
Marfatia T., van Eijk R., d'Adamo P., van Ruler M.A.J.H., Kuijjer M.L., Oosting J., Cleton-Jansen A.-M., van Oosterwijk J.G., Verbeke S.L.J., Meijer D., van Wezel T., 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., French P.J., Bovee J.V.M.G.
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.
Nat. Genet. 43:1256-1261(2011)