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Publication | Open Access

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

DOIFull Paper Access

250

Citations

27

References

2009

Year

Isabelle Audo, Susanne Kohl, Bart P. Leroy, Francis L. Munier, Xavier Guillonneau, Saddek Mohand‐Saïd, Kinga M. Bujakowska, Emeline F. Nandrot, Birgit Lorenz, Markus N. Preising,
The American Journal of Human Genetics

References

YearCitations

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