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Results: 1-3 |
Results: 3
Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness
Authors: Zeitz, Christina Jacobson, Samuel G. Hamel, Christian P. Bujakowska, Kinga
Citation: Zeitz, Christina et al., Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness, American journal of human genetics (Online) AJHG , 92(1), 2013, pp. 67-75
A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness
Authors: Riazuddin, S. Amer Shahzadi, Amber Zeitz, Christina Ahmed, Zubair M. Hejtmancik, J. Fielding
Citation: Riazuddin, S. Amer et al., A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness, American journal of human genetics (Online) AJHG , 87(4), 2010, pp. 523-531
Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness
Authors: Zeitz, Christina Kloeckener-Gruissem, Barbara Forster, Ursula Kohl, Susanne Magyar, István Wissinger, Bernd Mátyás, Gábor Borruat, François-Xavier Schorderet, Daniel F. Zrenner, Eberhart Munier, Francis L. Berger, Wolfgang
Citation: Zeitz, Christina et al., Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness, American journal of human genetics , 79(4), 2006, pp. 657-667
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