WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype

Published 2013 View Full Article

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Title
WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype
Authors
Keywords
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Journal
JOURNAL OF MEDICAL GENETICS
Volume 50, Issue 7, Pages 491-492
Publisher
BMJ
Online
2013-05-25
DOI
10.1136/jmedgenet-2013-101750
References
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