More on: Unusual expression of the F9 gene in peripheral lymphocytes hinders investigation of F9 mRNA in hemophilia patients [9]

Journal of Thrombosis and Haemostasis

Volumn 2, Issue 6, 2004, Pages 1021-

  Cutler, Jacqueline A ^a   Mitchell, Michael J ^a   Savidge, Geoffrey F ^a  

^a ST THOMAS HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 9; COMPLEMENTARY DNA; MESSENGER RNA;

CELLULAR DISTRIBUTION; EXON; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC TRANSCRIPTION; HEMOPHILIA B; HUMAN; LETTER; PATIENT REFERRAL; PERIPHERAL LYMPHOCYTE; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; RNA ANALYSIS;

FACTOR IX; HEMOPHILIA B; HUMANS; LYMPHOCYTES; RNA, MESSENGER;

EID: 19944433964     PISSN: 15387933     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2004.00724.x     Document Type: Letter

References (3)

1. Green PM, Rowley G, Giannelli F.. Unusual expression of the F9 gene in peripheral lymphocytes hinders investigation of F9 mRNA in hemophilia B patients. J Thromb Haemost 2003; 1: 2675-700.
2. Sarkar G, Sommer SS. Access to a messenger RNA sequence or its protein product is not limited by tissue or species specificity. Science 1989; 244: 331-4.
3. Chan V, Au P, Lau P, Chan TK. A novel haemophilia B defect due to partial duplication of the factor IX gene. Br J Haematol 1994; 86: 601-9.