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PR.2017.149
PR.2017.149
http://dx.doi.org/10.1038/PR.2017.149
Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3.
P356
Q40139592-1E651AF7-1C39-4D39-AEE6-3D86678261C3
P356
PR.2017.149
http://dx.doi.org/10.1038/PR.2017.149