TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness-Reference-Cited by-同舟云学术

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

Published:2009-11 Issue:5 Volume:85 Page:720-729
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference32 articles.

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