Two rare MPL gene mutations in patients with essential thrombocythemia

International Journal of Hematology

Volumn 90, Issue 3, 2009, Pages 431-432

  Ohashi, Haruhiko ^a   Arita, Kayoko ^a   Fukami, Shoko ^a   Oguri, Kayo ^a   Nagai, Hirokazu ^a   Yokozawa, Toshiya ^a   Hotta, Tomomitsu ^a   Hanada, Shuichi ^b  

^a NATIONAL HOSPITAL ORGANIZATION NAGOYA MEDICAL CENTER   (Japan)

^b NATIONAL HOSPITAL ORGANIZATION KAGOSHIMA MEDICAL CENTER   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; GLUTAMINE; LYSINE; PHENYLALANINE; PROLINE; THREONINE; TRYPTOPHAN;

AMINO ACID SUBSTITUTION; EXON; GENE; GENE INSERTION; GENE MUTATION; GRANULOCYTE; HUMAN; LETTER; MISSENSE MUTATION; MPL GENE; NUCLEOTIDE SEQUENCE; THROMBOTIC THROMBOCYTOPENIC PURPURA;

ADULT; FEMALE; GRANULOCYTES; HUMANS; MIDDLE AGED; MUTATION, MISSENSE; RECEPTORS, THROMBOPOIETIN; T-LYMPHOCYTES; THROMBOCYTHEMIA, ESSENTIAL;

EID: 76449107758     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12185-009-0413-3     Document Type: Letter

References (7)

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