Concepedia

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 M. Bujakowska, Emeline F. Nandrot, Birgit Lorenz, Markus N. Preising,

The American Journal of Human Genetics · 2009 · 262 citations · 27 references

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27

ISCEV Standard for full-field clinical electroretinography (2008 update)

Michael F. Marmor, Anne B. Fulton, Graham E. Holder et al. · Documenta Ophthalmologica · 2008 · 1K citations · Full text

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Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

Bech-Hansen Nt, Ben F. Koop, M. B. Mets et al. · Nature Genetics · 1998 · 518 citations

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An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

Tim M. Strom, Gerald Nyakatura, Eckart Apfelstedt-Sylla et al. · Nature Genetics · 1998 · 504 citations

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Congenital Stationary Night Blindness With Negative Electroretinogram

Yozo Miyake · Archives of Ophthalmology · 1986 · 456 citations

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Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells

Akinori Nomura, Ryuichi Shigemoto, Yasuhisa Nakamura et al. · Cell · 1994 · 439 citations

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