Hyperhomocyst(e)inemia and a common methylene-tetrahydrofolate reductase mutation (Ala223 Val MTHFR) are not associated with a history of thrombosis in patients with inherited thrombophilia

被引：0
|
作者：
Legnani, C
Palareti, G
Sassi, S
Grauso, F
Bargossi, A
Bernardi, F
Marchetti, G
Ferraresi, P
Coccheri, S
机构：
[1] UNIV FERRARA, DIPARTIMENTO BIOCHIM & BIOL MOL, I-44100 FERRARA, ITALY
[2] UNIV BOLOGNA, S ORSOLA M MALPIGHI HOSP, DEPT ANGIOL & BLOOD COAGULAT, CENT LAB, BOLOGNA, ITALY
来源：
THROMBOSIS AND HAEMOSTASIS | 1997年
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D O I：
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中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
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页码：P2325 / P2325
页数：1
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