SysPIMP: the web-based systematical platform for identifying human disease-related mutated sequences from mass spectrometry
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/37/suppl_1/D913/3314983/gkn848.pdf
Reference46 articles.
1. Position effect in human genetic disease
2. Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties 1 1Edited by J. Thornton
3. SNPs, protein structure, and disease
4. Towards a structural basis of human non-synonymous single nucleotide polymorphisms
5. Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: structure-based assessment of amino acid variation11Edited by F. Cohen
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