Orphanet: Diagnostik des Dravet Syndroms GEFS Typ 2 SCN1A Gen

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Diagnosis of Dravet syndrome / GEFS+ type 2 (SCN1A gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 21/12/2011
  • Abteilung für Neuropädiatrie, Sozialpädiatrie und Epileptologie
  • Kinderklinik des UKGM am Standort Gießen
  • Feulgenstraße 10-12
  • 35392 GIEßEN
  • Director of laboratory : -
  • More information
  • Phone : 49 (0)641 985 43481
  • Additional Phone : -
  • Fax : 49 (0)641 985 43489
  • Website
Last update: December 2011

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of genes tested (including panels) (1)
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