Orphanet: Diagnostik des Dravet Syndroms SCN1A Gen
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Diagnosis of Dravet syndrome (SCN1A gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 03/08/2009
  • Institut für Klinische Genetik und Tumorgenetik
  • MVZ Institut für Klinische Genetik und Tumorgenetik Bonn GmbH
  • Maximilianstrasse 28D
  • 53111 BONN
  • GERMANY
  • Director of laboratory : Dr Nicolai KOHLSCHMIDT
  • More information
  • Phone : 49 (0)228 96968670
  • Additional Phone : -
  • Fax : 49 (0)228 96968676
  • Website
  • Contact
Last update: August 2009

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

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

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.