Clinical and ERG data in a family with autosomal dominant RP and Pro-347-Arg mutation in the rhodopsin gene

Author:

Niemeyer G�nter,Tr�b Peter,Schinzel Albert,Gal Andreas

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Sensory Systems,Ophthalmology

Reference22 articles.

1. Inglehearn CF, Bashir R, Lester DH, Jay M, Bird AC, Bhattacharya SS. A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa. Am J Hum Genet 1991; 48: 26?30.

2. Dryja TP, McGee TL, Reichel E, Hahn LB, Cowley GS, Yandell DW, Sandberg MA, Berson EL. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Nature 1990; 343: 364?6.

3. Dryja TP, McGee TL, Hahn LB, Cowley GS, Olsson JE, Reichel E, Sandberg MA, Berson EL. Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa. N Engl J Med 1990; 323: 1302?7.

4. Dryja TP, Hahn LB, McGee TL, Cowley GS, Berson EL. Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa. Proc Natl Acad Sci USA 1991; 88: 9370?74.

5. Bhattacharya SS, Ingelhearn CF, Keen J, Lester D, Bashir R, Jay M, Bird AC. Identification of novel rhodopsin mutations in patients with autosomal dominant retinitis pigmentosa. Invest Ophthalmol Vis Sci 1991; 32(suppl): 890.

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