Author:
Bayes M,Goldaracena B,Martinez-Mir A,Iragui-Madoz M I,Solans T,Chivelet P,Bussaglia E,Ramos-Arroyo M A,Baiget M,Vilageliu L,Balcells S,Gonzalez-Duarte R,Grinberg D
Subject
Genetics(clinical),Genetics
Reference30 articles.
1. Clinical findings and common symptoms in retinitis pigmentosa;Heckenlively, JR, Yoser; SL, Friedman; LH, Oversier; J.J.;Am _J Ophthalmol,1988
2. Molecular genetics of retinitis pigmentosa;Dryja, T.P.; Li, T.;Hum Mol Genet,1995
3. A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa;Rosenfeld, P.J.; Cowley, G.S.; McGee, T.L.; Sandberg, M.A.; Berson, E.L.; Dryja, T.P.;Nat Genet,1992
4. Autosomal recessive retinitis pigmentosa caused by mutations in the a-subunit of rod cGMPphosphodiesterase;Huang, S.H.; Pittler, S.J.; Huang, X.H.; Oliveira, L.; Berson, E.L.; Dryja, T.P.;Nat Genet,1995
5. Recessive mutations in the gene encoding the P-subunit of rod phosphodiesterase in patients;McLaughlin, M.E.; Ehrhart, T.L.; Berson, E.L.; Dryja, T.P.,1995
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