These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
26. The phenotype of early-onset retinal degeneration in persons with RDH12 mutations. Schuster A, Janecke AR, Wilke R, Schmid E, Thompson DA, Utermann G, Wissinger B, Zrenner E, Gal A. Invest Ophthalmol Vis Sci; 2007 Apr; 48(4):1824-31. PubMed ID: 17389517 [Abstract] [Full Text] [Related]
35. Retinal dystrophies caused by mutations in RPE65: assessment of visual functions. Hamel CP, Griffoin JM, Lasquellec L, Bazalgette C, Arnaud B. Br J Ophthalmol; 2001 Apr; 85(4):424-7. PubMed ID: 11264131 [Abstract] [Full Text] [Related]
36. Leber's congenital amaurosis associated with high hyperopia in four sisters. Babel J, Klein D, Roth A. Ophthalmic Paediatr Genet; 1989 Mar; 10(1):55-61. PubMed ID: 2662098 [Abstract] [Full Text] [Related]
37. Leber congenital amaurosis--differential diagnosis, ophthalmological and neuroradiological report of 18 patients. Casteels I, Spileers W, Demaerel P, Casaer P, De Cock P, Dralands L, Missotten L. Neuropediatrics; 1996 Aug; 27(4):189-93. PubMed ID: 8892367 [Abstract] [Full Text] [Related]