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Q26853455-EB70BA33-2F3D-4E64-B7DF-5127B1D93C1B
Q26853455-EB70BA33-2F3D-4E64-B7DF-5127B1D93C1B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26853455-EB70BA33-2F3D-4E64-B7DF-5127B1D93C1B
Educational paper. Connective tissue disorders with vascular involvement: from gene to therapy
P2860
Q26853455-EB70BA33-2F3D-4E64-B7DF-5127B1D93C1B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26853455-EB70BA33-2F3D-4E64-B7DF-5127B1D93C1B
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
1ea1fa72dd3cc3bad7fed08cb7d9347126d76bd6
P2860
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2