Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-011-1115-5.pdf
Reference15 articles.
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2. Berger W, Kloeckener-Gruissema B, Neidhardt J (2010) The molecular basis of human retinal and vitreoretinal diseases. Prog Retin Eye Res 29:335–375
3. Boughman JA, Fishman GA (1983) A genetic analysis of retinitis pigmentosa. Br J Ophthalmol 67:449–454
4. Braverman N, Steel G, Obie C, Moser A, Moser H, Gould SJ, Valle D (1997) Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata. Nat Genet 15:369–376
5. Bundey S, Crews SJ (1984) A study of retinitis pigmentosa in the City of Birmingham I. Prevalence. J Med Genet 21:417–420
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