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Molecular diagnosis of Benign Familial Neonatal Seizures type 1 by Sequencing of the entire coding region of gene (s) / copy number analysis (KCNQ2 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 05/06/2014
  • 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: June 2014

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
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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.