Exome sequencing to identify causative variants of blood clot dysfunction

被引：0
|
作者：
Couzens, Alexander [1 ]
Neerman-Arbez, Marguerite [1 ]
机构：
[1] Univ Geneva, Dept Genet Med & Dev, Geneva, Switzerland
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷
基金：
瑞士国家科学基金会;
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P06.031.C
引用
收藏
页码：423 / 424
页数：2
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