Article
Calcium channels and channelopathies of the central nervous system.
Molecular neurobiology - 1 Feb 2002
Pietrobon Daniela
Abstract excerpt
Several inherited human neurological disorders can be caused by mutations in genes encoding Ca2+ channel subunits. This review deals with known human and mouse calcium channelopathies of the central nervous system (CNS). The human diseases comprise: 1) a recessive retinal disorder, X-linked congenital stationary night blindness, associated with mutations in the CACNA1F gene, encoding alpha(1)1.4 subunits of...
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