Orphanet: Postnatal molecular diagnosis of spinocerebellar ataxias type 1, 2, 6 and 7 ATXN1, ATXN2, CACNA1A and ATXN7 genes
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Postnatal molecular diagnosis of spinocerebellar ataxias type 1, 2, 6 and 7 (ATXN1, ATXN2, CACNA1A and ATXN7 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 12/06/2009
  • Molecular genetics Unit
  • Department of biology and medical genetics
  • Motol university hospital - 2nd Medical School Charles University Prague
  • V Uvalu 84
  • 150 06 PRAHA 5
  • CZECH REPUBLIC
  • Director of laboratory : Dr Anna KREPELOVA
  • More information
  • Phone : 420 224 433 501
  • Additional Phone : -
  • Fax : 420 224 433 520
  • Website
Last update: June 2009

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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List of diseases and genes

List of genes tested (including panels) (4)
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.