Methods for the detection of the JAK2 V617F mutation in human myeloproliferative disorders.

Methods in molecular medicine

Volumn 125, Issue , 2006, Pages 253-264

  Campbell, Peter J ^a   Scott, Linda M ^a   Baxter, E Joanna ^a   Bench, Anthony J ^a   Green, Anthony R ^a   Erber, Wendy N ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

JAK2 PROTEIN, HUMAN; JANUS KINASE 2; ONCOPROTEIN; PROTEIN TYROSINE KINASE;

AMINO ACID SUBSTITUTION; ARTICLE; DIFFERENTIAL DIAGNOSIS; GENETICS; HUMAN; METHODOLOGY; MISSENSE MUTATION; MYELOFIBROSIS; MYELOPROLIFERATIVE DISORDER; POLYCYTHEMIA VERA; POLYMERASE CHAIN REACTION; THROMBOCYTOSIS;

AMINO ACID SUBSTITUTION; DIAGNOSIS, DIFFERENTIAL; HUMANS; JANUS KINASE 2; MUTATION, MISSENSE; MYELOFIBROSIS; MYELOPROLIFERATIVE DISORDERS; POLYCYTHEMIA VERA; POLYMERASE CHAIN REACTION; PROTEIN-TYROSINE KINASES; PROTO-ONCOGENE PROTEINS; THROMBOCYTOSIS;

EID: 33645473018     PISSN: 15431894     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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