Generalized Inherited Retinal Dystrophies
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-12041-1_12
Reference110 articles.
1. Dryja, T.P., McGee, T.L., Reichel, E., et al.: A point mutation of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa. Nature 343, 364–366 (1990)
2. McWilliam, P., Farrar, G.J., Kenna, P., et al.: Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3. Genomics 5, 619–622 (1989)
3. Gregory-Evans, K., Bhattacharya,.S.S.: Genetic blindness: current concepts in the pathogenesis of human outer retinal dystrophies. Trends Genet. 14, 103–108 (1998)
4. Evans, D.M., Cardon, L.R.: Guidelines for genotyping in genome wide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps. Am. J. Hum. Genet. 75, 687–692 (2004)
5. Sullivan, L.S., Daiger, S.P.: Inherited retinal degeneration: exceptional genetic and clinical heterogeneity. Mol. Med. Today 2, 380–386 (1996)
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