Orphanet: Molecular diagnosis of Dravet syndrome SMEI SCN1A gene: whole gene sequencing analysis
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Molecular diagnosis of Dravet syndrome - SMEI (SCN1A gene: whole gene sequencing analysis)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 11/05/2011
  • West of Scotland Genetic Services
  • Laboratory Medicine (Level 2/B)
  • Queen Elizabeth University Hospital
  • 1345 Govan Road
  • GLASGOW G51 4TF
  • UNITED KINGDOM
  • Director of laboratory : Dr Nicola WILLIAMS
  • More information
  • Phone : 44 (0)141 354 9300
  • Additional Phone : 44 (0)141 354 9408 / 9410
  • Fax : 44 (0)141 232 7980
  • Website
  • Contact
Last update: May 2011

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)
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.