Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome-Reference-Cited by-同舟云学术

Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome

Published:2022-05-23 Issue:10 Volume:7 Page:
ISSN:2379-3708
Container-title:JCI Insight
language:en
Short-container-title:

Author:

McQuaid Mary E.^ORCID,Ahmed Kashif,Tran Stephanie,Rousseau Justine^ORCID,Shaheen Ranad^ORCID,Kernohan Kristin D.,Yuki Kyoko E.^ORCID,Grover Prerna^ORCID,Dreseris Ema S.,Ahmed Sameen,Dupuis Lucie^ORCID,Stimec Jennifer,Shago Mary,Al-Hassnan Zuhair N.^ORCID,Tremblay Roch^ORCID,Maass Philipp G.^ORCID,Wilson Michael D.,Grunebaum Eyal,Boycott Kym M.,Boisvert François-Michel^ORCID,Maddirevula Sateesh^ORCID,Faqeih Eissa A.,Almanjomi Fahad,Khan Zaheer Ullah,Alkuraya Fowzan S.^ORCID,Campeau Philippe M.^ORCID,Kannu Peter,Campos Eric I.^ORCID,Wurtele Hugo^ORCID

Funder

Natural Sciences and Engineering Research Council of Canada

Canadian Institutes of Health Research

King Fahad Medical City

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://insight.jci.org/articles/view/155648/files/pdf

Reference70 articles.

1. Isolation of the Cdc45/Mcm2-7/GINS (CMG) complex, a candidate for the eukaryotic DNA replication fork helicase