Rhodopsin and autosomal dominant retinitis pigmentosa

Author:

Dryja Thaddeus P

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology

Reference67 articles.

1. Chen JD, Halliday F, Keith G, Sheffield L, Dickinson P, Gray R, Constable I, Denton M : Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci. Am J Hum Genet 1989, 45: 401–11.

2. Kimberling Wl, Moller CG, Davenport SLH, Lund G, Grissom TJ, Priluck I, White V, Weston MD, Biscone-Halterman K, Brookhouser PE : Usher syndrome: clinical findings and gene localisation studies. Laryngoscope 1988, 99: 66–72.

3. Kimberling WJ, Weston MD, Moller C, Davenport SL, Shugart YY, Priluck JA, Martini A, Milani M, Smith RJ : Localisation of Usher syndrome type II to chromosome 1q. Genomics 1990, 7: 245–9.

4. Kolb, J and Gouras P : Electron microscopic observations of human retinitis pigmentosa, dominantly inherited. Invest Ophthalmol Vis Sci 1974, 13: 487–98.

5. Verhoeff FH : Microscopic observations in a case of retinitis pigmentosa. Arch Ophthalmol 1931, 5: 392–407.

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