A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.
Chapman J; Rees E; Harold D; Ivanov D; Gerrish A; Sims R; Hollingworth P; Stretton A; Holmans P; Owen MJ; O'Donovan MC; Williams J; Kirov G; Human Molecular Genetics, 2013, vol. 22, issue 4, p 816, ISSN 14602083. ISBN 14602083.

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