Orphanet: Diagn�stico de la hemiplej�a alternante de la infancia genes ATP1A2, ATP1A3
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Diagnosis of alternating hemiplegia of childhood (ATP1A2, ATP1A3 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 14/10/2014
  • Instituto de Medicina Genmica
  • IMEGEN - Delegacin Valencia
  • Calle Catedrtico Agustn Escardino, 9
  • 46980 PATERNA
  • SPAIN
  • Director of laboratory : Dr Juan LPEZ SILES
  • More information
  • Phone : 34 963212340
  • Additional Phone : -
  • Fax : -
  • Website
  • Contact
Last update: October 2014

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

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

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.