Molecular Mechanisms of Disease-Causing Missense Mutations
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Structural Biology
Reference194 articles.
1. Overlapping genomic sequences: a treasure trove of single-nucleotide polymorphisms;Taillon-Miller;Genome Res,1998
2. SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants;De Baets;Nucleic Acids Res,2012
3. Eye colour: portals into pigmentation genes and ancestry;Sturm;Trends Genet,2004
4. Bioinformatics challenges for personalized medicine;Fernald;Bioinformatics,2011
5. Bioinformatics approaches and resources for single nucleotide polymorphism functional analysis;Mooney;Brief Bioinform,2005
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