A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.
Chapman, Jade; Rees, Elliott; Harold, Denise; Ivanov, Dobril; Gerrish, Amy; Sims, Rebecca; Hollingworth, Paul; Stretton, Alexandra; Holmans, Peter; Owen, Michael J.; O'Donovan, Michael C.; Williams, Julie; Kirov, George; Human Molecular Genetics, 2013, vol. 22, issue 4, p 816, ISSN 09646906. ISBN 14602083.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef