Cockayne syndrome without UV-sensitivity in Vietnamese siblings with novel ERCC8 variants-Reference-Cited by-同舟云学术

Cockayne syndrome without UV-sensitivity in Vietnamese siblings with novel ERCC8 variants

Published:2022-06-22 Issue:13 Volume:14 Page:5299-5310
ISSN:1945-4589
Container-title:Aging
language:en
Short-container-title:Aging

Author:

Duong Nguyen Thuy¹,Dinh Tran Huu¹,Möhl Britta S.²,Hintze Stefan³,Quynh Do Hai¹,Ha Duong Thi Thu¹,Ngoc Ngo Diem⁴,Dung Vu Chi⁴,Miyake Noriko⁵⁶,Hai Nong Van¹,Matsumoto Naomichi⁵,Meinke Peter³

Affiliation:

1. Institute of Genome Research, Vietnam Academy of Science and Technology, Hanoi, Vietnam

2. Institute of Virology, School of Medicine, Technical University of Munich/Helmholtz Zentrum München, Munich, Germany

3. Friedrich-Baur-Institute, Department of Neurology, LMU Klinikum, Ludwig-Maximilians-University Munich, Munich, Germany

4. Vietnam National Children’s Hospital, Hanoi, Vietnam

5. Department of Human Genetics, Yokohama City University Graduate School of Medicine, Kanagawa, Japan

6. Department of Human Genetics, Research Institute, National Center for Global Health and Medicine, Tokyo, Japan

Publisher

Impact Journals, LLC

Subject

Cell Biology,Aging

Reference32 articles.

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2. The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care.;Motojima;Genet Med,2016

3. Cockayne syndrome: the expanding clinical and mutational spectrum.;Laugel;Mech Ageing Dev,2013

4. Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.;Martin-Coignard;Hum Mutat,2010

5. The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH.;Friedberg;Cell,1995

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