Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
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England: BioMed Central Ltd
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English
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England: BioMed Central Ltd
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Osteoporosis is a complex disease with a strong genetic contribution. A recently published genome-wide association study (GWAS) for estimated bone mineral density (eBMD) identified 1103 independent genome-wide significant association signals. Most of these variants are non-coding, suggesting that regulatory effects may drive many of the association...
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Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
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TN_cdi_doaj_primary_oai_doaj_org_article_5bd008c3bef74c23b6dda461abaf7c6f
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5bd008c3bef74c23b6dda461abaf7c6f
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ISSN
1474-760X,1474-7596
E-ISSN
1474-760X
DOI
10.1186/s13059-020-01997-2
