Orphanet: Molecular diagnosis of SCA7: Spinocerebellar ataxia type 7 ATXN7 gene

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Molecular diagnosis of SCA7: Spinocerebellar ataxia type 7 (ATXN7 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 24/11/2009
  • Laboratory for Molecular Diagnostics
  • Department of Human Genetics
  • University Hospitals Leuven - Gasthuisberg
  • Herestraat 49
  • 3000 LEUVEN
  • Director of laboratory : Pr Gert MATTHIJS
  • More information
  • Phone : +32 (0)16 3 46 062
  • Additional Phone : -
  • Fax : +32 (0)16 3 46 060
  • Website
Last update: November 2009

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
PCR based techniques

List of diseases and genes

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

Quality management


EQA scheme(s) organized by EMQN

SCA (Spinocerebellar ataxias)
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.