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TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

✍ Scribed by Isabelle Audo; Susanne Kohl; Bart P. Leroy; Francis L. Munier; Xavier Guillonneau; Saddek Mohand-Saïd; Kinga Bujakowska; Emeline F. Nandrot; Birgit Lorenz; Markus Preising; Ulrich Kellner; Agnes B. Renner; Antje Bernd; Aline Antonio; Veselina Moskova-Doumanova; Marie-Elise Lancelot; Charlotte M. Poloschek; Isabelle Drumare; Sabine Defoort-Dhellemmes; Bernd Wissinger; Thierry Léveillard; Christian P. Hamel; Daniel F. Schorderet; Elfride De Baere; Wolfgang Berger; Samuel G. Jacobson; Eberhart Zrenner; José-Alain Sahel; Shomi S. Bhattacharya; Christina Zeitz

Book ID: 113422716
Publisher: American Society of Human Genetics
Year: 2009
Tongue: English
Weight: 760 KB
Volume: 85
Category: Article
ISSN: 0002-9297
DOI: 10.1016/j.ajhg.2009.10.013

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