A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions-Reference-Cited by-同舟云学术

A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions

Published:2020-10 Issue:4 Volume:107 Page:654-669
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Garg Paras,Jadhav Bharati,Rodriguez Oscar L.,Patel Nihir,Martin-Trujillo Alejandro,Jain Miten,Metsu Sofie,Olsen Hugh,Paten Benedict,Ritz Beate,Kooy R. Frank,Gecz Jozef,Sharp Andrew J.

Funder

Universiteit Antwerpen

American Heart Association

National Institute of Neurological Disorders and Stroke

Foundation for the National Institutes of Health

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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