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Association of common candidate variants with vascular malformations and intracranial hemorrhage in hereditary hemorrhagic telangiectasia.

Ludmila PawlikowskaJeffrey NelsonDiana E GuoCharles E McCullochMichael T LawtonHelen KimMarie E Faughnannull null
Published in: Molecular genetics & genomic medicine (2018)
We did not replicate previously reported associations with HHT lung AVM and variants in Tgfb modifier loci. We also did not find significant associations between variants reported in sporadic brain AVM and VM or ICH in HHT.
Keyphrases
  • copy number
  • genome wide
  • white matter
  • late onset
  • gene expression
  • dna methylation
  • multiple sclerosis
  • blood brain barrier
  • brain injury
  • subarachnoid hemorrhage