Orphanet: Molekulare Diagnostik der Hemiplegia alternans ATP1A2 und ATP1A3 Gen

Search for a diagnostic test

* (*) mandatory field

Molecular diagnosis of alternating hemiplegia (ATP1A2 and ATP1A3 genes)

  • Institut für Medizinische Genetik
  • Zentrum für Pathobiochemie und Genetik
  • Medizinische Universität Wien
  • 1090 WIEN
  • Director of laboratory : Pr Franco LACCONE
  • More information
  • Phone : +43 (0)1 40160 56531
  • Additional Phone : +43 (0)1 40160 956531
  • Fax : -
  • Website
Last update: December 2017

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (2)
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.