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Journal description
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Details for article 23 of 23 found articles
| Title: |
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness |
| Author: |
Audo, Isabelle Bujakowska, Kinga Orhan, Elise Poloschek, Charlotte M. Defoort-Dhellemmes, Sabine Drumare, Isabelle Kohl, Susanne Luu, Tien D. Lecompte, Odile Zrenner, Eberhart Lancelot, Marie-Elise Antonio, Aline Germain, Aurore Michiels, Christelle Audier, Claire Letexier, Mélanie Saraiva, Jean-Paul Leroy, Bart P. Munier, Francis L. Mohand-Saïd, Saddek Lorenz, Birgit Friedburg, Christoph Preising, Markus Kellner, Ulrich Renner, Agnes B. Moskova-Doumanova, Veselina Berger, Wolfgang Wissinger, Bernd Hamel, Christian P. Schorderet, Daniel F. De Baere, Elfride Sharon, Dror Banin, Eyal Jacobson, Samuel G. Bonneau, Dominique Zanlonghi, Xavier Le Meur, Guylene Casteels, Ingele Koenekoop, Robert Long, Vernon W. Meire, Francoise Prescott, Katrina de Ravel, Thomy Simmons, Ian Nguyen, Hoan Dollfus, Hélène Poch, Olivier Léveillard, Thierry Nguyen-Ba-Charvet, Kim Sahel, José-Alain Bhattacharya, Shomi S. Zeitz, Christina |
| Appeared in: |
The American journal of human genetics |
| Paging: | Volume 91 (2012) nr. 1 pages 1 p. |
| Year: |
2012 |
| Contents: | |
| Publisher: |
The American Society of Human Genetics |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 23 of 23 found articles
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