DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Pawlikowska L, Nelson J, Guo DE. et al; Brain Vascular Malformation Consortium HHT Investigator Group.
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.
Am J Med Genet A 2015;
167 (06) 1262-1267
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