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Q37644369-095717BF-273D-4C2F-AF62-33ED64DE80D8
Q37644369-095717BF-273D-4C2F-AF62-33ED64DE80D8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37644369-095717BF-273D-4C2F-AF62-33ED64DE80D8
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
P2860
Q37644369-095717BF-273D-4C2F-AF62-33ED64DE80D8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37644369-095717BF-273D-4C2F-AF62-33ED64DE80D8
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
a8eae73f5349cf26ec1877d77b2f352bba0d0d35
P2860
Freeman-Sheldon syndrome (whistling face syndrome) and cranio-vertebral junction malformation producing dysphagia and weight loss.