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Q37644369-3C29F774-1C70-429A-92A1-68EA4B79F17B
Q37644369-3C29F774-1C70-429A-92A1-68EA4B79F17B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37644369-3C29F774-1C70-429A-92A1-68EA4B79F17B
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
P2860
Q37644369-3C29F774-1C70-429A-92A1-68EA4B79F17B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37644369-3C29F774-1C70-429A-92A1-68EA4B79F17B
rank
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type
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wasDerivedFrom
f0992bf440278b86de2ccdfd482411479090f8f5
P2860
Expanded clinical spectrum of spondylocarpotarsal synostosis syndrome and possible manifestation in a heterozygous father