Lon R Cardon1. Show Affiliations » 1. Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK. lon.cardon@well.ox.ac.uk
Abstract
Mesh: See more » Case-Control StudiesCrohn Disease/geneticsGenetic HeterogeneityGenetic Predisposition to DiseaseGenetic Testing/methodsGenome, HumanHumansMacular Degeneration/geneticsNod2 Signaling Adaptor Protein/geneticsPhenotypePolymorphism, Single NucleotideReceptors, Interleukin/geneticsSample Size
Substances: See more » IL23R protein, humanNOD2 protein, humanNod2 Signaling Adaptor ProteinReceptors, Interleukin
Year: 2006 PMID: 17138888 DOI: 10.1126/science.1136668
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728