Orphanet: Diagnosi molecolare dell_epilessia mioclonica grave del neonato gene SCN1A
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Molecular diagnosis of Dravet syndrome (SCN1A gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 12/07/2010
  • Laboratorio di Genetica Molecolare 1
  • Istituto di Scienze Neurologiche
  • CNR
  • Contrada Burga
  • 87050 MANGONE (CS)
  • ITALY
  • Director of laboratory : Pr Grazia ANNESI
  • More information
  • Phone : 39 0984 9801248
  • Additional Phone : 39 0984 9801233
  • Fax : 39 0984 969306
  • Website
Last update: July 2010

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (1)
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