The majority of the genetic risk for Paget’s disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes

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Title
The majority of the genetic risk for Paget’s disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes
Authors
Keywords
-
Journal
HUMAN GENETICS
Volume 128, Issue 6, Pages 615-626
Publisher
Springer Nature
Online
2010-09-13
DOI
10.1007/s00439-010-0888-2

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