Orphanet: Diagn�stico molecular de enxaqueca hemipl�gica familiar painel NGS para os genes ATP1A2, CACNA1A, PRRT2, SCN1A: Sequencia��o de toda a regi�o codificante

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Molecular diagnosis of familial hemiplegic migraine (NGS panel for genes ATP1A2, CACNA1A, PRRT2, SCN1A: Sequencing of the entire coding region)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 04/08/2014
  • Centro de Gentica Preditiva e Preventiva
  • Instituto de Biologia Molecular e Celular
  • Rua do Campo Alegre, 823
  • 4150-180 PORTO
  • Director of laboratory : Pr Jorge SEQUEIROS
  • More information
  • Phone : 351 226 074 942
  • Additional Phone : -
  • Fax : 351 226 002 923
  • Website
  • Contact
Last update: August 2014

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)

List of diseases and genes

List of genes tested (including panels) (4)

Additional information

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