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    EIG3 Epilepsy, idiopathic generalized, susceptibility to 3 [ Homo sapiens (human) ]

    Gene ID: 432400, updated on 31-Aug-2024

    Summary

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    Official Symbol
    EIG3provided by HGNC
    Official Full Name
    Epilepsy, idiopathic generalized, susceptibility to 3provided by HGNC
    Primary source
    MIM:608762
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Genomic context

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    Location:
    9q32-q33

    Bibliography

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    Related articles in PubMed

    1. Autosomal recessive idiopathic epilepsy in an inbred family from Turkey: identification of a putative locus on chromosome 9q32-33. Baykan B, et al. Epilepsia, 2004 May. PMID 15101829

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    Epilepsy, idiopathic generalized, susceptibility to 3
    OMIM: 608762GeneReviews: Not available

    General gene information

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    Markers

    Property

    • phenotype only

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