Premium
Evaluation of mutations in the isocitrate dehydrogenase genes in therapy‐related and secondary acute myeloid leukaemia identifies a patient with clonal evolution to IDH2 R172K homozygosity due to uniparental disomy
Author(s) -
Pichler Monika M.,
Bodner Claudia,
Fischer Carina,
Deutsch Alexander J.,
Hiden Karin,
BehamSchmid Christine,
Linkesch Werner,
Guelly Christian,
Sill Heinz,
Wölfler Albert
Publication year - 2011
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.2010.08404.x
Subject(s) - idh1 , idh2 , isocitrate dehydrogenase , uniparental disomy , myelodysplastic syndromes , myeloid , cancer research , bone marrow , biology , medicine , mutation , oncology , genetics , gene , karyotype , enzyme , biochemistry , chromosome