Nucleic acid encoding SCN1A variant

A method of identifying a subject predisposed to a disorder associated with ion channel dysfunction, comprising ascertaining whether at least one of the genes encoding ion channel subunits in said subject has undergone a mutation event such that a cDNA derived from said subject has the sequence set...

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Bibliographische Detailangaben
Hauptverfasser: HERON SARAH ELIZABETH, HARKIN LOUISE ANNE, WALLACE ROBYN HEATHER, PHILLIPS HILARY ANNE, MULLEY JOHN CHARLES, SCHEFFER INGRID EILEEN, BERKOVIC SAMUEL FRANK, DIBBENS LEANNE MICHELLE
Format: Patent
Sprache:eng
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