| Title : Homozygosity for R87H missense mutation and for a rare intron 7 DNA variant (7054G -->\; A) in the PROC genes of three siblings initially classified as heterozygotes for protein C deficiency - Soria_1996_Blood.Coagul.Fibrinolysis_7_15 |
| Author(s) : Soria JM , Morell M , Nicolau I , Estivill X , Sala N |
| Ref : Blood Coagul Fibrinolysis , 7 :15 , 1996 |
| Abstract : Soria_1996_Blood.Coagul.Fibrinolysis_7_15 |
| ESTHER : Soria_1996_Blood.Coagul.Fibrinolysis_7_15 |
| PubMedSearch : Soria_1996_Blood.Coagul.Fibrinolysis_7_15 |
| PubMedID: 8845458 |
Soria JM, Morell M, Nicolau I, Estivill X, Sala N (1996)
Homozygosity for R87H missense mutation and for a rare intron 7 DNA variant (7054G -->\; A) in the PROC genes of three siblings initially classified as heterozygotes for protein C deficiency
Blood Coagul Fibrinolysis
7 :15
Soria JM, Morell M, Nicolau I, Estivill X, Sala N (1996)
Blood Coagul Fibrinolysis
7 :15