Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice

Mammalian Genome

Volumn 8, Issue 2, 1997, Pages 113-120

  Doyle, Johannah ^a   Ren, Xiaojia ^a   Lennon, Greg ^b   Stubbs, Lisa ^a  

^a OAK RIDGE NATIONAL LABORATORY   (United States)

^b LAWRENCE LIVERMORE NATIONAL LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CACNA1A PROTEIN, HUMAN; CACNA1A PROTEIN, MOUSE; CACNA1A PROTEIN, RAT; CALCIUM CHANNEL; CALCIUM CHANNEL P TYPE; CALCIUM CHANNEL Q TYPE; COMPLEMENTARY DNA;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; CEREBELLAR ATAXIA; CEREBELLUM; CHROMOSOME 19; CHROMOSOME MAP; DNA SEQUENCE; GENE EXPRESSION; GENETICS; HUMAN; METABOLISM; MIGRAINE; MOLECULAR GENETICS; MOUSE; MOUSE MUTANT; MUTATION; RAT; SEIZURE; SEQUENCE HOMOLOGY; SPINOCEREBELLAR DEGENERATION;

AMINO ACID SEQUENCE; ANIMALS; CALCIUM CHANNELS; CALCIUM CHANNELS, P-TYPE; CALCIUM CHANNELS, Q-TYPE; CEREBELLAR ATAXIA; CEREBELLUM; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 19; DNA, COMPLEMENTARY; GENE EXPRESSION; HUMANS; MICE; MICE, NEUROLOGIC MUTANTS; MIGRAINE DISORDERS; MOLECULAR SEQUENCE DATA; MUTATION; RATS; SEIZURES; SEQUENCE ANALYSIS, DNA; SEQUENCE HOMOLOGY, AMINO ACID; SPINOCEREBELLAR DEGENERATIONS;

ANIMALIA; ATAXIA; RODENTIA;

EID: 0031064169     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900369     Document Type: Article

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