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Q35552797-DD1D25B4-82C7-46A6-ABE5-8DBB81B6B2B9
Q35552797-DD1D25B4-82C7-46A6-ABE5-8DBB81B6B2B9
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http://www.wikidata.org/entity/statement/Q35552797-DD1D25B4-82C7-46A6-ABE5-8DBB81B6B2B9
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.
P2860
Q35552797-DD1D25B4-82C7-46A6-ABE5-8DBB81B6B2B9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35552797-DD1D25B4-82C7-46A6-ABE5-8DBB81B6B2B9
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Statement
wasDerivedFrom
9e67084c2e8f529d32d40c8551b2399b20b7c376
P2860
Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35