Concepedia

Congenital Stationary Night Blindness in Mice – A Tale of Two Cacna1f Mutants

N. Lodha, Stephan Bonfield, Noelle C. Orton, Clinton J. Doering, John E. McRory, Silvina C. Mema, Renata Rehak, Yves Sauvé, Rose Tobias, William K. Stell,

Advances in experimental medicine and biology · 2009 · 40 citations · 22 references

DOI

Concepts

References

22

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

, , +12

The Presynaptic Active Zone Protein Bassoon Is Essential for Photoreceptor Ribbon Synapse Formation in the Retina

Oliver Dick, Susanne tom Dieck, Wilko Detlef Altrock et al. · Neuron · 2003 · 467 citations · Full text

, , +14

Congenital Stationary Night Blindness With Negative Electroretinogram

Yozo Miyake · Archives of Ophthalmology · 1986 · 456 citations

, , +15

Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function

Françoise Haeseleer, Yoshikazu Imanishi, Tadao Maeda et al. · Nature Neuroscience · 2004 · 294 citations · Full text

, , +17