Nucleic Acid Encoding Scn1a Variant

Abstract

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 forth in one of SEQ ID NOS: 1-134.


Claims
Owners (US)
IPC Classifications
Download PDF
Document Preview
Document History
  • Publication: Aug 2, 2011
  • Application: Jan 29, 2010
    US US 69676910 A
  • Priority: Jan 29, 2010
    US US 69676910 A
  • Priority: Oct 12, 2004
    US US 48283404 A
  • Priority: Jul 8, 2002
    AU AU 1910/002009 W
  • Priority: May 13, 2002
    AU AU PS229202 A
  • Priority: Mar 5, 2002
    AU AU PS091002 A
  • Priority: Jul 18, 2001
    AU AU PR645201 A

Sign in to the Lens

Feedback