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Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis.

    Citation

    Elmslie FV, Hutchings SM, Spencer V, et al
    Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis.

    Publication history

    • First published May 1, 1996.
    Online issue publication 
    May 01, 1996

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