Orphanet: Molecular diagnosis of autosomal dominant spinocerebellar ataxia SCA 1, 2, 3, 6, 7 and 8: CAG expansion
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Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7 and 8): CAG expansion

Despite our efforts to ensure that data is up to date, this activity has not been validated since 12/12/2011
  • Institüt für Medizinische Molekulargenetik
  • Universität Zürich
  • Wagistrasse 12
  • 8952 SCHLIEREN
  • SWITZERLAND
  • Director of laboratory : Pr Wolfgang BERGER
  • More information
  • Phone : 0041 (0)44 556 33 50
  • Additional Phone : -
  • Fax : 0041 (0)44 556 33 51
  • Website
  • Contact
Last update: December 2011

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
PCR based techniques
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Quality management

EQA
 EQA

EQA scheme(s) organized by EMQN

SCA (Spinocerebellar ataxias)
2014
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