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TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness
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. ReVolume:
85
Année:
2009
Langue:
english
Pages:
10
DOI:
10.1016/j.ajhg.2009.10.013
Fichier:
PDF, 760 KB
english, 2009