Orphanet: Molecular Diagnosis of Spinocerebellar Ataxia type 7 ATXN7 triplet repeat analysis
x

Search for a diagnostic test

* (*) mandatory field

Molecular Diagnosis of Spinocerebellar Ataxia type 7 (ATXN7 triplet repeat analysis)

  • NYGH Cytogenetics and Molecular Genetics Laboratory
  • North York General Hospital
  • 4001 Leslie Street
  • M2K 1E1 TORONTO
  • CANADA
  • Director of laboratory : Dr Hong WANG
  • More information
  • Phone : 1(416)756-6791
  • Additional Phone : -
  • Fax : 1(416)756-6792
  • Website
Last update: January 2018

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis
Pre-symptomatic 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)
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.