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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

✍ Scribed by Albagha, Omar M E; Visconti, Micaela R; Alonso, Nerea; Langston, Anne L; Cundy, Tim; Dargie, Rosemary; Dunlop, Malcolm G; Fraser, William D; Hooper, Michael J; Isaia, Gianluca


Book ID
109914590
Publisher
Nature Publishing Group
Year
2010
Tongue
English
Weight
713 KB
Volume
42
Category
Article
ISSN
1061-4036

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