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

页码：27 / 28

页数：2

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