Orphanet: Diagnosi molecolare postnatale della emiplegia alternante dell_infanzia analisi del gene ATP1A2 mediante sequenziamento dell_intera regione codificante
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Post-natal molecular diagnosis of alternating hemiplegia of childhood (sequence analysis of the entire coding region of ATP1A2 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 23/10/2015
  • 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 diseases tested (1)
List of genes tested (including panels) (1)
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