Orphanet: Molecular diagnosis of generalized epilepsy with febrile seizures plus context GABRG2, SCN1A, SCN1B and SCN2A gene sequencing
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Molecular diagnosis of generalized epilepsy with febrile seizures-plus context (GABRG2, SCN1A, SCN1B and SCN2A gene sequencing)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 23/07/2009
  • Phone : 45 66 11 66 28
  • Additional Phone : -
  • Fax : 45 66 11 66 78
  • Website
Last update: July 2009

Responsible of diagnostic test

Purpose(s)

Antenatal diagnosis
Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
Sanger sequencing
Mutation scanning/screening and sequence analysis of selected exons
NGS sequencing (except WES)
Sequence analysis: entire coding region
NGS sequencing (except WES)

List of diseases and genes

List of genes tested (including panels) (4)
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