Raine Syndrome (OMIM #259775), Caused By FAM20C Mutation, Is Congenital Sclerosing Osteomalacia With Cerebral Calcification (OMIM 259660)
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Title
Raine Syndrome (OMIM #259775), Caused By FAM20C
Mutation, Is Congenital Sclerosing Osteomalacia With Cerebral Calcification (OMIM 259660)
Authors
Keywords
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Journal
JOURNAL OF BONE AND MINERAL RESEARCH
Volume 32, Issue 4, Pages 757-769
Publisher
Wiley
Online
2016-11-10
DOI
10.1002/jbmr.3034
References
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