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Article

A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus

16 Dec 2013

Abstract excerpt

BACKGROUND: Osteoporosis is a systemic skeletal disease characterised by reduced bone mineral density and increased susceptibility to fracture; these traits are highly heritable. Both common and rare copy number variants (CNVs) potentially affect the function of genes and may influence disease risk. AIM: To identify CNVs associated with osteoporotic bone fracture risk. METHOD: We performed a genome-wide CNV...

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PMID: 24343915
DOI: 10.1136/jmedgenet-2013-102064

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