Orphanet: Diagnosi molecolare postnatale delle convulsioni infantili benigne analisi dei geni SCN2A e PRRT2 mediante sequenziamento dell_intera regione codificante
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Post-natal molecular diagnosis of benign familial infantile epilepsy (sequence analysis of the entire coding region of SCN2A and PRRT2 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 25/10/2015
  • Laboratorio di Neurogenetica
  • Clinica di Neurologia Pediatrica
  • Azienda Ospedaliera Universitaria Anna Meyer
  • Viale Pieraccini 24
  • 50139 FIRENZE
  • ITALY
  • Director of laboratory : Pr Renzo GUERRINI
  • More information
  • Phone : 39 055 5662844
  • Additional Phone : 39 055 5662573
  • Fax : 39 055 5662329
  • Website
Last update: October 2015

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 genes tested (including panels) (1)
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