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Electroretinography as a screening method for mutations causing retinal dysfunction in mice.
Dalke C, Löster J, Fuchs H, Gailus-Durner V, Soewarto D, Favor J, Neuhäuser-Klaus A, Pretsch W, Gekeler F, Shinoda K, Zrenner E, Meitinger T, Hrabé de Angelis M, Graw J. Dalke C, et al. Among authors: favor j. Invest Ophthalmol Vis Sci. 2004 Feb;45(2):601-9. doi: 10.1167/iovs.03-0561. Invest Ophthalmol Vis Sci. 2004. PMID: 14744904
A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice.
Sidjanin DJ, Parker-Wilson DM, Neuhäuser-Klaus A, Pretsch W, Favor J, Deen PM, Ohtaka-Maruyama C, Lu Y, Bragin A, Skach WR, Chepelinsky AB, Grimes PA, Stambolian DE. Sidjanin DJ, et al. Among authors: favor j. Genomics. 2001 Jun 15;74(3):313-9. doi: 10.1006/geno.2001.6509. Genomics. 2001. PMID: 11414759
158 results