Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness (vol 90, pg 321, 2012) Isabelle Audo , Kinga Bujakowska , Elise Orhan , Charlotte M. Poloschek , Sabine Defoort-Dhellemmes , Isabelle Drumare , Susanne Kohl , Tien D. Luu , Odile Lecompte , Eberhart Zrenner , Marie-Elise Lancelot , Aline Antonio , Aurore Germain , Christelle Michiels , Claire Audier , Melanie Letexier , Jean-Paul Saraiva , Bart P. Leroy , Francis L. Munier , Saddek Mohand-Said , Birgit Lorenz , Christoph Friedburg , Markus Preising , Ulrich Kellner , Agnes B. Renner , Veselina Moskova-Doumanova , Wolfgang Berger , Bernd Wissinger , Christian P. Hamel , Daniel F. Schorderet , Elfride De Baere , Dror Sharon , Eyal Banin , Samuel G. Jacobson , Dominique Bonneau , Xavier Zanlonghi , Guylene Le Meur , Ingele Casteels , Robert Koenekoop , Vernon W. Long , Francoise Meire , Katrina Prescott , Thomy de Ravel , Ian Simmons , Hoan Nguyen , Helene Dollfus , Olivier Poch , Thierry Leveillard , Kim Nguyen-Ba-Charvet , Jose-Alain Sahel , Shomi S. Bhattacharya , Christina Zeitz The American Journal of Human Genetics(2012)
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