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Q37644369-37E676E3-CE6A-47DF-9661-329162B471E3
Q37644369-37E676E3-CE6A-47DF-9661-329162B471E3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37644369-37E676E3-CE6A-47DF-9661-329162B471E3
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
P2860
Q37644369-37E676E3-CE6A-47DF-9661-329162B471E3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37644369-37E676E3-CE6A-47DF-9661-329162B471E3
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wasDerivedFrom
af36a56d78781122f01b80e011fb3292d43576ae
P2860
The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscle