Information Journal Paper
APA:
CopyLEGNANI, C., PALARETI, G., GRAUSO, F., SASSI, S., GROSSI, G., & PIAZZI, S.. (1997). HYPERHOMOCYST (E) INEMIA AND A COMMON METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION (ALA 223 VAL, MTHFR) IN PATIENTS
WITH INHERITED THROMBOPHILIC COAGULATION EFFECTS
. ARTERIOSCLEROSIS, THROMBOSIS, AND VASCULAR BIOLOGY, 17(-), 2924-2929. SID. https://sid.ir/paper/538509/en
Vancouver:
CopyLEGNANI C., PALARETI G., GRAUSO F., SASSI S., GROSSI G., PIAZZI S.. HYPERHOMOCYST (E) INEMIA AND A COMMON METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION (ALA 223 VAL, MTHFR) IN PATIENTS
WITH INHERITED THROMBOPHILIC COAGULATION EFFECTS
. ARTERIOSCLEROSIS, THROMBOSIS, AND VASCULAR BIOLOGY[Internet]. 1997;17(-):2924-2929. Available from: https://sid.ir/paper/538509/en
IEEE:
CopyC. LEGNANI, G. PALARETI, F. GRAUSO, S. SASSI, G. GROSSI, and S. PIAZZI, “HYPERHOMOCYST (E) INEMIA AND A COMMON METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION (ALA 223 VAL, MTHFR) IN PATIENTS
WITH INHERITED THROMBOPHILIC COAGULATION EFFECTS
,” ARTERIOSCLEROSIS, THROMBOSIS, AND VASCULAR BIOLOGY, vol. 17, no. -, pp. 2924–2929, 1997, [Online]. Available: https://sid.ir/paper/538509/en