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Q52691549-0A2F070F-DB6A-46C7-A596-1C5CD30FE096
Q52691549-0A2F070F-DB6A-46C7-A596-1C5CD30FE096
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http://www.wikidata.org/entity/statement/Q52691549-0A2F070F-DB6A-46C7-A596-1C5CD30FE096
A novel MAP3K7 splice mutation causes cardiospondylocarpofacial syndrome with features of hereditary connective tissue disorder.
P2860
Q52691549-0A2F070F-DB6A-46C7-A596-1C5CD30FE096
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52691549-0A2F070F-DB6A-46C7-A596-1C5CD30FE096
rank
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type
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Statement
wasDerivedFrom
633cf54a0bb5be4b8edb62a7624d2f0310c5e6cf
P2860
Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia