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Q40205509-33498C20-E171-474B-9B13-6E198CB4CD8C
Q40205509-33498C20-E171-474B-9B13-6E198CB4CD8C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40205509-33498C20-E171-474B-9B13-6E198CB4CD8C
Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion in ACVRL1 Suggests the Causing Mechanism.
P2860
Q40205509-33498C20-E171-474B-9B13-6E198CB4CD8C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40205509-33498C20-E171-474B-9B13-6E198CB4CD8C
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
82246ade4996f5f67d71f11a542c9564a90f8089
P2860
A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).