Orphanet: Diagnosi molecolare dell_epilessia mioclonica grave del neonato geni SCN1A, SCN1B e GABRG2
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Molecular diagnosis of severe myoclonic epilepsy of infancy (SCN1A, SCN1B and GABRG2 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 29/09/2010
  • U.O.C. di Medicina Molecolare
  • Dipartimento dei Servizi
  • Azienda Ospedaliera Universitaria Senese - Ospedale Santa Maria alle Scotte
  • Viale Mario Bracci
  • 53100 SIENA
  • ITALY
  • Director of laboratory : Pr Vincenzo SORRENTINO
  • More information
  • Phone : 39 0577 234192
  • Additional Phone : 39 0577 586261
  • Fax : 39 0577 234191
  • Website
  • Contact
Last update: September 2010

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) (3)
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