Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy

Míreanna Comhchosúla

• Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy
  le: Poulter, James A., et al.
  Foilsithe: (2010)
• Autosomal dominant exudative vitreoretinopathy.
  le: Ober, R R, et al.
  Foilsithe: (1980)
• Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree
  le: Toomes, C, et al.
  Foilsithe: (2005)
• Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree
  le: Toomes, C, et al.
  Foilsithe: (2005)
• A New Locus for Autosomal Dominant Familial Exudative Vitreoretinopathy Maps to Chromosome 11p12-13
  le: Downey, L. M., et al.
  Foilsithe: (2001)