Genetic Variation Associated with Coeliac Disease
The present invention provides a method of diagnosing coeliac disease, said method comprising analysing a sample of nucleic acid from a human subject to determine the presence or absence of one or more single nucleic polymorphisms (SNPs) in one or more human chromosomal regions selected from the group consisting of Iq31, 2ql l-2ql2, 3p21, 3q25-3q26, 3q28, 6q25 and 12q24.
VAN HEEL DAVID [GB]; HUNT KAREN [GB]; WIJMENGA CISCA [NL]; MCMANUS OWEN ROSS [IE]; DELOUKAS PANAGIOTIS [GB]
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