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

the Brain Vascular Malformation Consortium HHT Investigator Group

Research output: Contribution to journal › Article › peer-review

17 Scopus citations

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Medicine & Life Sciences