Analysis of ALK-1 and endoglin in newborns from families with hereditary hemorrhagic telangiectasia type 2

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Oxford University Press

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Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion in ACVRL1 Suggests the Causing Mechanism

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Expression analysis of endoglin missense and truncation mutations: insights into protein structure and disease mechanisms

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Oxford University Press

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The ACVRL1 c.314—35A>G polymorphism is associated with organ vascular malformations in hereditary hemorrhagic telangiectasia patients with ENG mutations, but not in patients with ACVRL1 mutations

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A mouse model for hereditary hemorrhagic telangiectasia (HHT) type 2

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