Orphanet: Diagnostik des Dravet Syndroms SCN1A Gen: Sequenzierung MLPA
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Diagnosis of Dravet syndrome (SCN1A gene: sequencing / MLPA)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 22/07/2015
  • bio.logis Zentrum für Humangenetik
  • bio.logis Zentrum für Humangenetik
  • Altenhöferallee 3
  • 60438 FRANKFURT AM MAIN
  • GERMANY
  • Director of laboratory : Pr Daniela STEINBERGER
  • More information
  • Phone : 49 (0)69 530 8437 0
  • Additional Phone : -
  • Fax : 49 (0)69 530 8437 11
  • Website
  • Contact
Last update: July 2015

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
Deletion / Duplication analysis
MLPA based techniques

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.