Classification of mismatch repair gene missense variants with PON-MMR
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference66 articles.
1. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs;Altschul;Nucleic Acids Res,1997
2. A method and server for predicting damaging missense mutations;Adzhubei;Nat Methods,2010
3. nsSNPAnalyzer: identifying disease-associated nonsynonymous single nucleotide polymorphisms;Bao;Nucleic Acids Res,2005
4. Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2;Betz;J Cancer Res Clin Oncol,2010
5. SNAP: predict effect of non-synonymous polymorphisms on function;Bromberg;Nucleic Acids Res,2007
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