Misexpression of inactive genes is associated with nearby rare structural variants

被引：0
|
作者：
Vanderstichele, Thomas [1 ]
Burnham, Katie L. [1 ]
de Klein, Niek [1 ]
Howell, Brittany [1 ]
Walter, Klaudia [1 ]
Kundu, Kousik [1 ,2 ]
Nath, Artika [2 ,3 ]
Persyn, Elodie [2 ]
Marten, Jonathan [2 ]
Roberts, David [4 ]
Di Angelantonio, Emanuele [2 ]
Danesh, John [2 ]
Berton, Alix [5 ]
Platt, Adam [5 ]
Butterworth, Adam [2 ]
Soranzo, Nicole [1 ]
Parts, Leopold [1 ]
Inouye, Michael [2 ,3 ]
Paul, Dirk [2 ,6 ]
Davenport, Emma [1 ]
机构：
[1] Wellcome Sanger Inst, Cambridge, England
[2] Univ Cambridge, Cambridge, England
[3] Baker Heart & Diabet Inst, Melbourne, Vic, Australia
[4] Univ Oxford, Oxford, England
[5] AstraZeneca, Translat Sci & Expt Med, Res & Early Dev, Resp & Immunol, Cambridge, England
[6] AstraZeneca, Ctr Genom Res, Discovery Sci, BioPharmaceut R&D, Cambridge, England
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32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：
C09.4
引用
收藏
页码：27 / 28
页数：2
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