Orphanet: Diagnostik der alternierenden Hemiplegie des Kindesalters ATP1A3 Gen: Sequenzierung
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Diagnosis of alternating hemiplegia of childhood (ATP1A3 gene: sequencing)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 08/01/2013
  • Stoffwechsel- und DNA-Labor der Kinderklinik
  • Zentrum Kinderheilkunde und Jugendmedizin - Abteilung Pädiatrie II
  • Universitätsmedizin Göttingen
  • Robert-Koch-Str. 40
  • 37099 GÖTTINGEN
  • GERMANY
  • Director of laboratory : Dr Ralph KRÄTZNER
  • More information
  • Phone : 49 (0)551 39 13657
  • Additional Phone : 49 (0)551 39 22972
  • Fax : -
  • Website
  • Contact
Last update: January 2013

Responsible of diagnostic test

Purpose(s)

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) (1)

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.