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Genome-wide association study identifies variants at CSF1... | ResearchHub
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Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone
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Authors
Omar Albagha
16 more
Omar Albagha
•
Micaela Visconti
14 more
•
Stuart Ralston
Published
May 2, 2010
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Journal
Nature Genetics
Topics
Biology
Bioinformatics
Medicine
Cancer Oncology
Pathology
Show all topics
DOI
10.1038/ng.562
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Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Nature Genetics
Topics
Biology
Bioinformatics
Medicine
Cancer Oncology
Pathology
Show all topics
DOI
10.1038/ng.562
Other Formats
PDF