New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene

Author:

Sakamoto Kenji,McCluskey Michael,Wensel Theodore G.,Naggert Jürgen K.,Nishina Patsy M.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference36 articles.

1. Retinitis pigmentosa;Hartong;Lancet,2006

2. Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase;Huang;Nat. Genet.,1995

3. Recessive mutations in the gene encoding the beta-subunit of rod phophodiesterase in patients with retinitis pigmentosa;McLaughlin;Nat. Genet.,1993

4. Frequency of mutations in the gene encoding the alpha subunit of rod cGMP-phosphodiesterase in autosomal recessive retinitis pigmentosa;Dryja;Invest. Ophthalmol. Vis. Sci.,1999

5. Stationary night blindness or progressive retinal degeneration in mice carrying different alleles of PDE gamma;Farber;Front. Biosci.,2003

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