PTHR1 mutations associated with Ollier disease result in receptor loss of function

Published 2008 View Full Article

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Title
PTHR1 mutations associated with Ollier disease result in receptor loss of function
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 17, Issue 18, Pages 2766-2775
Publisher
Oxford University Press (OUP)
Online
2008-06-18
DOI
10.1093/hmg/ddn176
References
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