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TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness

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Description scientific article
Author/s

author: Susanne Kohl  Marie-Elise Lancelot  Veselina Moskova-Doumanova  Agnes B Renner  Aline Antonio  Charlotte M Poloschek  Sabine Defoort-Dhellemmes  Samuel G. Jacobson  Thierry Léveillard  Isabelle Audo  Xavier Guillonneau  Elfride De Baere  Bernd Wissinger  José-Alain Sahel  Saddek Mohand-Saïd  Markus Preising  Kinga Bujakowska  Bart Leroy  Christina Zeitz 

Publication date November 5, 2009
Language English
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