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
  • PORTUGAL
  • 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

Purpose(s)

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

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.