Patterns and Mutational Signatures of Tandem Base Substitutions Causing Human Inherited Disease-Reference-Cited by-同舟云学术

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Patterns and Mutational Signatures of Tandem Base Substitutions Causing Human Inherited Disease

Published:2013-05-20 Issue:8 Volume:34 Page:1119-1130
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Chen Jian-Min¹²³,Férec Claude¹²³⁴,Cooper David N.⁵

Affiliation:

1. Institut National de la Santé et de la Recherche Médicale (INSERM); Brest France

2. Etablissement Français du Sang (EFS) - Bretagne; Brest France

3. Faculté de Médecine et des Sciences de la Santé; Université de Bretagne Occidentale (UBO); Brest France

4. Laboratoire de Génétique Moléculaire et d'Histocompatibilité, Centre Hospitalier Universitaire (CHU) Brest; Hôpital Morvan; Brest France

5. Institute of Medical Genetics, School of Medicine; Cardiff University; Cardiff United Kingdom

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22341/fullpdf

Reference67 articles.

1. An integrated map of genetic variation from 1,092 human genomes;Abecasis;Nature,2012

2. Mutator phenotypes due to DNA replication infidelity;Arana;Semin Cancer Biol,2010

3. Head and neck cancer;Argiris;Lancet,2008

4. Evidence for a high frequency of simultaneous double-nucleotide substitutions;Averof;Science,2000

5. Sequence analysis of mutations and translocations across breast cancer subtypes;Banerji;Nature,2012

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