Genomewide association study identifies no major founder variant in Caucasian moyamoya disease

J Genet. 2013 Dec;92(3):605-9. doi: 10.1007/s12041-013-0304-5.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Case-Control Studies
  • DNA Mutational Analysis
  • European Continental Ancestry Group / genetics
  • Female
  • Founder Effect
  • Genome-Wide Association Study
  • Humans
  • Male
  • Moyamoya Disease / ethnology
  • Moyamoya Disease / genetics*
  • Polymorphism, Single Nucleotide
  • Young Adult