Isolation and Characterization of a Calcium Channel Gene, Cacna1f, the Murine Orthologue of the Gene for Incomplete X-Linked Congenital Stationary Night Blindness

Molecular cloning: A laboratory manual

Prescott L. Deininger · Analytical Biochemistry · 1990 · 86.2K citations

Life Sciences, Molecular Biology, Molecular Genetics +11

Primary structure of the receptor for calcium channel blockers from skeletal muscle

Tsutomu Tanabe, Hiroshi Takeshima, Atsushi Mikami et al. · Nature · 1987 · 1.4K citations

Life Sciences, Biochemistry, Physiology +16

Calmodulin Is the Ca2+ Sensor for Ca2+-Dependent Inactivation of L-Type Calcium Channels

Blaise Z. Peterson, Carla D. DeMaria, David T. Yue · Neuron · 1999 · 851 citations · Full text

Life Sciences, Biochemistry, Cell Biology +17

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

Life Sciences, Genetics, Molecular Genetics +14

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

Life Sciences, Genetics, Molecular Genetics +12