A novel mutation of the protein C gene with a frameshift deletion of 3 base pair (3380AGG) in exon 6 in type 1 deficiency associated with arterial and venous thrombosis [2]

American Journal of Hematology

Volumn 62, Issue 4, 1999, Pages 260-261

  Takahashi, T ^a   Shinohara, K ^a   Nawata, R ^a   Wakiyama, M ^a   Hamasaki, N ^a  

^a Yamaguchi Central Hospital   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; DNA DETERMINATION; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; HUMAN; LETTER; MISSENSE MUTATION; PEDIGREE ANALYSIS; PRIORITY JOURNAL; PROTEIN C DEFICIENCY; THROMBOPHILIA;

FEMALE; FRAMESHIFT MUTATION; GENE DELETION; HUMANS; MIDDLE AGED; PEDIGREE; PROTEIN C; THROMBOSIS; VENOUS THROMBOSIS;

EID: 0032728331     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8652(199912)62:4<260::AID-AJH14>3.0.CO;2-8     Document Type: Letter

References (6)