References
- Warburg M. Heterogeneity of congenital retinal non-attachment, falciform folds and retinal dysplasia. A guide to genetic counselling.Hum Hered 1976;26:137–148.
- Warburg M. Doyne Memorial Lecture, 1979. Retinal malformations: aetiological heterogeneity and morphological similarity in congenital retinal non-attachment and falciform folds. Trans Ophthalmol Soc U K 1979; 99:272–283.
- Ghiasvand NM, Rudolph DD, Mashayekhi M, et al. Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease. Nat Neurosci 2011;14:578–586.
- Ghiasvand NM, Shirzad E, Naghavi M, et al. High incidence of autosomal recessive nonsyndromal congenital retinal nonattachment (NCRNA) in an Iranian founding population. Am J Med Genet 1998;78:226–232.
- Phillips CI, Stokoe NL. Congenital hereditary bilateral nonattachment of retina: a sibship of two males. J Pediatr Ophthalmol Strabismus 1979;16:358–363.
- Ohba N, Watanabe S, Fujita S. Primary vitreoretinal dysplasia transmitted as an autosomal recessive disorder. Br J Ophthalmol 1981;65:631–635.
- Prasov L, Masud T, Khaliq S, et al. ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. Hum Mol Genet 2012;21:3681–3694.
- Khan K, Logan CV, McKibbin M, et al. Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects. Hum Mol Genet 2012;21:776–783.
- Ye X, Wang Y, Nathans J. The Norrin/Frizzled4 signaling pathway in retinal vascular development and disease. Trends Mol Med 2010;16:417–425.
- Collin RW, Nikopoulos K, Dona M, et al. ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature. Proc Natl Acad Sci U S A 2013;110:9856–9861.
- Brown NL, Dagenais SL, Chen CM, et al. Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development. Mamm Genome 2002;13:95–101.