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Q52724465-616DCAB2-96CC-4DBD-AD46-6EDF091A8546
Q52724465-616DCAB2-96CC-4DBD-AD46-6EDF091A8546
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52724465-616DCAB2-96CC-4DBD-AD46-6EDF091A8546
A novel pathogenic MYH3 mutation in a child with Sheldon-Hall syndrome and vertebral fusions.
P2860
Q52724465-616DCAB2-96CC-4DBD-AD46-6EDF091A8546
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52724465-616DCAB2-96CC-4DBD-AD46-6EDF091A8546
rank
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Statement
wasDerivedFrom
5873850f8f8d082dde517a34eb943c037ff3a556
P2860
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.