A nonsense mutation of human XRCC 4 is associated with adult‐onset progressive encephalocardiomyopathy-Reference-Cited by-同舟云学术

A nonsense mutation of human XRCC 4 is associated with adult‐onset progressive encephalocardiomyopathy

Published:2015-04-14 Issue:7 Volume:7 Page:918-929
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Bee Leonardo¹,Nasca Alessia²,Zanolini Alice²,Cendron Filippo¹,d'Adamo Pio³,Costa Rodolfo¹,Lamperti Costanza²,Celotti Lucia¹,Ghezzi Daniele²,Zeviani Massimo²⁴

Affiliation:

1. Department of Biology University of Padua Padua Italy

2. Molecular Neurogenetics Unit Foundation IRCCS Institute of Neurology “Carlo Besta” Milan Italy

3. Department of Medical Sciences University of Trieste Trieste Italy

4. MRC Mitochondrial Biology Unit, CB2 0XY Cambridge UK

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201404803

Reference51 articles.

1. The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates

2. XLF Interacts with the XRCC4-DNA Ligase IV Complex to Promote DNA Nonhomologous End-Joining

3. Involvement of Poly(ADP-ribose) Polymerase-1 and XRCC1/DNA Ligase III in an Alternative Route for DNA Double-strand Breaks Rejoining

4. The Efficiency of Homologous Recombination and Non-Homologous End Joining Systems in Repairing Double-Strand Breaks during Cell Cycle Progression

5. Is Non-Homologous End-Joining Really an Inherently Error-Prone Process?

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