Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse

Podobne zapisy

• The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification
  od: Cross, Sally H., i wsp.
  Wydane: (2020)
• Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmos
  od: Khorram, David, i wsp.
  Wydane: (2015)
• Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort
  od: Prasov, Lev, i wsp.
  Wydane: (2020)
• Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function
  od: Findlay, Amy S., i wsp.
  Wydane: (2020)
• The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype
  od: Cross, Sally H., i wsp.
  Wydane: (2011)