ASXL1 mutated chronic myelomonocytic leukemia in a patient with familial thrombocytopenia secondary to germline mutation in ANKRD26. Blood Cancer J 2015 May 22;5(5):e315
Date
05/23/2015Pubmed ID
26001113Pubmed Central ID
PMC4476020DOI
10.1038/bcj.2015.41Scopus ID
2-s2.0-84989920080 (requires institutional sign-in at Scopus site) 33 CitationsAuthor List
Perez Botero J, Oliveira JL, Chen D, Reichard KK, Viswanatha DS, Nguyen PL, Pruthi RK, Majerus J, Gada P, Gangat N, Tefferi A, Patnaik MMAuthor
Juliana Perez Botero MD Assistant Professor in the Medicine department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
Chromosome BreakageChromosome Disorders
Germ-Line Mutation
Humans
Intercellular Signaling Peptides and Proteins
Leukemia, Myelomonocytic, Chronic
Male
Middle Aged
Nuclear Proteins
Repressor Proteins
Thrombocytopenia
