Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia-Reference-Cited by-同舟云学术

Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia

Published:2013-05 Issue:5 Volume:92 Page:800-806
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Bogliolo Massimo,Schuster Beatrice,Stoepker Chantal,Derkunt Burak,Su Yan,Raams Anja,Trujillo Juan P.,Minguillón Jordi,Ramírez María J.,Pujol Roser,Casado José A.,Baños Rocío,Rio Paula,Knies Kerstin,Zúñiga Sheila,Benítez Javier,Bueren Juan A.,Jaspers Nicolaas G.J.,Schärer Orlando D.,de Winter Johan P.,Schindler Detlev,Surrallés Jordi

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype;Stoepker;Nat. Genet.,2011

2. Mutations of the SLX4 gene in Fanconi anemia;Kim;Nat. Genet.,2011

3. A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network;Antonio Casado;J. Med. Genet.,2007

4. FANCM connects the genome instability disorders Bloom’s Syndrome and Fanconi Anemia;Deans;Mol. Cell,2009

5. The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif;Enzlin;EMBO J.,2002

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