Low frequency of JAK2 exon 12 mutations in classic and atypical CMPDs

Leukemia Research

Volumn 32, Issue 9, 2008, Pages 1485-1487

  Ormazabal C ^a   Hurtado, C ^a   Aranaz, P ^a   Erquiaga, I ^a   Garcia Delgado M ^a   Calasanz, M J ^a   Novo, F J ^a   Vizmanos, J L ^a  

^a UNIVERSITY OF NAVARRA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE; JANUS KINASE 2; PROTEIN TYROSINE KINASE;

CELL CLONE; CELL PROLIFERATION; CELL SURVIVAL; EXON; GENE AMPLIFICATION; GENE DELETION; GENE FREQUENCY; GENE SEQUENCE; GENETIC CODE; GENETIC VARIABILITY; HEMATOLOGIC MALIGNANCY; HETEROZYGOSITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; LETTER; MYELOPROLIFERATIVE DISORDER; PRIORITY JOURNAL; PROMOTER REGION; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; SOMATIC MUTATION;

CHRONIC DISEASE; EXONS; HUMANS; JANUS KINASE 2; MUTATION; MYELOPROLIFERATIVE DISORDERS; POLYCYTHEMIA VERA;

EID: 43049161336     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2008.01.002     Document Type: Letter

References (8)

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8. Pardanani A., Lasho T.L., Finke C., Hanson C.A., and Tefferi A. Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera. Leukemia 21 9 (2007) 1960-1963