Orphanet: Molecular diagnosis of Alternating Hemiplegia of Childhood ATP1A3 gene
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Molecular diagnosis of Alternating Hemiplegia of Childhood (ATP1A3 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 30/03/2017
  • Sectie DNA diagnostiek
  • Afdeling Klinische Genetica
  • Erasmus MC, Faculteitsgebouw
  • Dr. Molewaterplein 50
  • 3015 GE ROTTERDAM
  • NETHERLANDS
  • Director of laboratory : Dr E.H. [Lies] HOEFSLOOT
  • More information
  • Phone : +31 (0)10 704 3197
  • Additional Phone : -
  • Fax : +31 (0)10 704 3200
  • Website
  • Contact
Last update: March 2017

Purpose(s)

Post-natal diagnosis
Pre-symptomatic 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) (1)
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.