A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia
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Title
A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 24, Issue 12, Pages 3399-3409
Publisher
Oxford University Press (OUP)
Online
2015-03-11
DOI
10.1093/hmg/ddv088
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Note: Only part of the references are listed.- Long-term observation of a patient with dominant omodysplasia
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