Inherited mutations in the helicase RTEL1 cause telomere dysfunction and Hoyeraal–Hreidarsson syndrome-Reference-Cited by-同舟云学术

Inherited mutations in the helicase RTEL1 cause telomere dysfunction and Hoyeraal–Hreidarsson syndrome

Published:2013-08-19 Issue:36 Volume:110 Page:E3408-E3416
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proc Natl Acad Sci USA

Author:

Deng Zhong,Glousker Galina,Molczan Aliah,Fox Alan J.,Lamm Noa,Dheekollu Jayaraju,Weizman Orr-El,Schertzer Michael,Wang Zhuo,Vladimirova Olga,Schug Jonathan,Aker Memet,Londoño-Vallejo Arturo,Kaestner Klaus H.,Lieberman Paul M.,Tzfati Yehuda

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference46 articles.

1. Telomeric Strategies: Means to an End

2. In Brief

3. Telomeres and telomerase in cancer

4. Shelterin: the protein complex that shapes and safeguards human telomeres

5. Telosome, a Mammalian Telomere-associated Complex Formed by Multiple Telomeric Proteins

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