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Q28118637-3D5ACAFA-3B72-415B-A25A-C2C26489A839
Q28118637-3D5ACAFA-3B72-415B-A25A-C2C26489A839
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28118637-3D5ACAFA-3B72-415B-A25A-C2C26489A839
Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease
P2860
Q28118637-3D5ACAFA-3B72-415B-A25A-C2C26489A839
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28118637-3D5ACAFA-3B72-415B-A25A-C2C26489A839
rank
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type
BestRank
Statement
wasDerivedFrom
7abefa5e144998ad169763c53203d0c42fe31262
P2860
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene