Concepedia

Mutations in the Gene KCNV2 Encoding a Voltage-Gated Potassium Channel Subunit Cause “Cone Dystrophy with Supernormal Rod Electroretinogram” in Humans

Huimin Wu, Jill A. Cowing, Michel Michaelides, Susan E. Wilkie, Glen Jeffery, Sharon Jenkins, Viktória Mester, Alan C. Bird, Anthony G. Robson, Graham E. Holder,

The American Journal of Human Genetics · 2006 · 137 citations · 13 references

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13

KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation

Yi-Han Chen, Shi-Jie Xu, Saı̈d Bendahhou et al. · Science · 2003 · 1K citations

, , +17

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes

Michael F. Waters, Natali A. Minassian, Giovanni Stévanin et al. · Nature Genetics · 2006 · 313 citations

, , +12

Obligatory heterotetramerization of three previously uncharacterized Kv channel α-subunits identified in the human genome

Natacha Ottschytsch, Adam Raes, Diane Van Hoorick et al. · Proceedings of the National Academy of Sciences · 2002 · 171 citations

, , +14

Cone Dystrophy, Nyctalopia, and Supernormal Rod Responses

Peter Gouras · Archives of Ophthalmology · 1983 · 131 citations

, , +17

Sequence-Function Analysis of the K+-Selective Family of Ion Channels Using a Comprehensive Alignment and the KcsA Channel Structure

Robin T. Shealy, Anuradha D. Murphy, Rampriya Ramarathnam et al. · Biophysical Journal · 2003 · 122 citations · Full text

, , +17