Mutation Screening of the GUCA1B Gene in Patients with Autosomal Dominant Cone and Cone Rod Dystrophy

By Kitiratschky Veronique B. D.   Glööckner Christian Johannes   Kohl Susanne  

Ophthalmic Genetics, Vol. 32, Iss. 3, 2011-09 ,pp. : 151-155

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Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease

By Kniazeva Marina   Chiang Michael F.   Cutting Garry R.   Zack Donald J.   Han Min   Zhang Kang  

Ophthalmic Genetics, Vol. 20, Iss. 2, 1999-06 ,pp. : 71-81

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Short-wave Cone Signal in the Red-Green Detection Mechanism

By Stromeyer C.F.   Chaparro A.   Rodriguez C.   Chen D.   Hu E.   Kronauer R.E.  

Vision Research, Vol. 38, Iss. 6, 1998-03 ,pp. : 813-826

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Topographical cone photopigment gene expression in deutan-type red-green color vision defects

By Bollinger K.   Sjoberg S.A.   Neitz M.   Neitz J.  

Vision Research, Vol. 44, Iss. 2, 2004-01 ,pp. : 135-145

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Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the family

By Van Ghelue Marijke   Eriksen Hans L.   Ponjavic Vesna   Fagerheim Toril   Andréasson Sten   Forsman-Semb Kristina   Sandgren Ola   Holmgren Gösta   Tranebjærg Lisbeth  

Ophthalmic Genetics, Vol. 21, Iss. 4, 2000-12 ,pp. : 197-209

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