A novel missense variant in the CAPN5 gene has been identified as associated with autosomal dominant neovascular inflammatory vitreoretinopathy. This discovery may enhance understanding of the genetic underpinnings of this rare eye disease.
novel capn5 missense variant associated with autosomal dominant neovascular inflammatory vitreoretinopathy
Original title: “A novel CAPN5 missense variant associated with autosomal dominant neovascular inflammatory vitreoretinopathy.”