Genetics in Medicine Open (Jan 2024)

P657: Structural variants identified by short-read genome sequencing solves missing heritability in retinal dystrophies

  • Ehsan Ullah,
  • Amelia Naik,
  • Chelsea Bender,
  • Delphine Blain,
  • Laryssa Huryn,
  • Robert Hufnagel,
  • Bin Guan

Journal volume & issue
Vol. 2
p. 101562

Abstract

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