Orphanet: Molecular Diagnosis of Spinocerebellar Ataxia Types 1,2,6,7,8 ATXN1, ATXN2, CACNA1A, ATXN7, ATXN8OS triplet repeat analysis
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Molecular Diagnosis of Spinocerebellar Ataxia Types 1,2,6,7,8 (ATXN1, ATXN2, CACNA1A, ATXN7, ATXN8OS triplet repeat analysis)

  • Molecular Diagnostic Laboratory
  • Diagnostic Services of Manitoba
  • Health Sciences Centre
  • 820 Sherbrook Street
  • R3A 1R9 WINNIPEG
  • CANADA
  • Director of laboratory : Dr Elizabeth SPRIGGS
  • More information
  • Phone : 1(204)787-1024
  • Additional Phone : 1(204)787-4033
  • Fax : 1(204)787-3846
  • Website
  • Contact
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
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.