Molecular investigation of 41 patients affected by coagulation factor XI deficiency

被引：8

作者：

Rimoldi, V. ^{[1
]}

Paraboschi, E. M. ^{[2
]}

Menegatti, M. ^{[3
]}

Peyvandi, F. ^{[3
,4
]}

Salomon, O. ^{[5
,6
]}

Duga, S. ^{[1
,2
]}

Asselta, R. ^{[1
,2
]}

机构：

[1] Humanitas Clin & Res Ctr, Milan, Italy

[2] Humanitas Univ, Dept Biomed Sci, Milan, Italy

[3] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Angelo Bianchi Bonomi Haemophilia & Thrombosis Ct, Milan, Italy

[4] Univ Milan, Dept Pathophysiol & Transplantat, Milan, Italy

[5] Chaim Sheba Med Ctr, Inst Thrombosis & Hemostasis, Tel Hashomer, Israel

[6] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel

来源：

HAEMOPHILIA | 2018年 / 24卷 / 02期

关键词：

POLYMERASE-CHAIN-REACTION; ASHKENAZI JEWS; MUTATIONS;

D O I：

10.1111/hae.13378

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：E50 / E55

页数：6

共 10 条

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[10] Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians [J].

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