| Literature DB >> 20403315 |
Jon McClellan1, Mary-Claire King.
Abstract
Strong evidence suggests that rare mutations of severe effect are responsible for a substantial portion of complex human disease. Evolutionary forces generate vast genetic heterogeneity in human illness by introducing many new variants in each generation. Current sequencing technologies offer the possibility of finding rare disease-causing mutations and the genes that harbor them. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
Mesh:
Year: 2010 PMID: 20403315 DOI: 10.1016/j.cell.2010.03.032
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582