Whole-genome sequencing identifies associations of sequence variants with clinically relevant urinary disease markers

被引：0
|
作者：
Benonisdottir, S. [1 ]
Oddsson, A. [1 ]
Sulem, G. [1 ]
Kristjansson, R. P. [1 ]
Olafsson, I. [2 ]
Onundarson, P. T. [2 ]
Kehr, B. [1 ]
Arnadottir, G. A. [1 ]
Holm, H. [1 ]
Masson, G. [1 ]
Edvardsson, V. O. [2 ,3 ]
Palsson, R. [2 ]
Jonasdottir, A. [1 ]
Jonasdottir, A. [1 ]
Mikaelsdottir, E. [1 ]
Eyjolfsson, G. I. [4 ]
Jensson, B. O. [1 ]
Thorsteinsdottir, U. [1 ,3 ]
Gudbjartsson, D. F. [1 ,5 ]
Sulem, P. [1 ]
Stefansson, K. [1 ,3 ]
机构：
[1] deCODE GeneticsAmgen Inc, Reykjavik, Iceland
[2] Landspitali Univ Hosp, Reykjavik, Iceland
[3] Univ Iceland, Fac Med, Reykjavik, Iceland
[4] Iceland Med Ctr Laeknasetrid, Lab Mjodd RAM, Reykjavik, Iceland
[5] Univ Iceland, Sch Engn & Nat Sci, Reykjavik, Iceland
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26卷
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：
C18.3
引用
收藏
页码：92 / 93
页数：2
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