Calcium channels and channelopathies of the central nervous system

Molecular Neurobiology

Volumn 25, Issue 1, 2002, Pages 31-50

  Pietrobon, Daniela ^a  

^a UNIVERSITY OF PADOVA   (Italy)

Author keywords

Ataxia; Calcium channel; Cerebellum; Channelopathy; Epilepsy; Genotypephenotype; Migraine; Mouse mutants; Mutation; Neurodegeneration

Indexed keywords

CALCIUM CHANNEL; CALCIUM CHANNEL L TYPE; CALCIUM CHANNEL Q TYPE; CACNA1A PROTEIN, HUMAN; CACNA1A PROTEIN, MOUSE; CACNA1F PROTEIN, HUMAN; CALCIUM; CALCIUM CHANNEL P TYPE; NERVE PROTEIN; PROTEIN SUBUNIT;

ANIMAL EXPERIMENT; ANIMAL MODEL; ATAXIA; AUTOSOMAL DOMINANT DISORDER; CENTRAL NERVOUS SYSTEM; CONTROLLED STUDY; EPILEPSY; GENE MUTATION; GENETIC CODE; GENOTYPE; LETHARGY; MIGRAINE; MOUSE; MOUSE MUTANT; NEUROLOGIC DISEASE; NIGHT BLINDNESS; NONHUMAN; PHENOTYPE; RETINA DISEASE; REVIEW; X CHROMOSOME RECESSIVE DISORDER; AMINO ACID SUBSTITUTION; ANIMAL; CALCIUM SIGNALING; CENTRAL NERVOUS SYSTEM DISEASE; CHANNEL GATING; CLASSIFICATION; DOMINANT GENE; GENETICS; HEMIPLEGIA; HUMAN; ION TRANSPORT; METABOLISM; MUTATION; PHYSIOLOGY;

AMINO ACID SUBSTITUTION; ANIMALS; ATAXIA; CALCIUM; CALCIUM CHANNELS; CALCIUM CHANNELS, L-TYPE; CALCIUM CHANNELS, P-TYPE; CALCIUM CHANNELS, Q-TYPE; CALCIUM SIGNALING; CENTRAL NERVOUS SYSTEM; CENTRAL NERVOUS SYSTEM DISEASES; EPILEPSY; GENES, DOMINANT; HEMIPLEGIA; HUMANS; ION CHANNEL GATING; ION TRANSPORT; MICE; MICE, NEUROLOGIC MUTANTS; MIGRAINE DISORDERS; MUTATION; NERVE TISSUE PROTEINS; NIGHT BLINDNESS; PHENOTYPE; PROTEIN SUBUNITS;

EID: 0036175714     PISSN: 08937648     EISSN: None     Source Type: Journal    
DOI: 10.1385/mn:25:1:031     Document Type: Review

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