Orphanet: Diagnosis of autosomal dominant spinocerebellar ataxia ATXN1,ATXN10,PPP2R2B,TBP , ATXN2,ATXN3,CACNA1A,ATXN7,ATXN8 genes
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Diagnosis of autosomal dominant spinocerebellar ataxia (ATXN1,ATXN10,PPP2R2B,TBP , ATXN2,ATXN3,CACNA1A,ATXN7,ATXN8 genes)

  • Genetica AG
  • Humangenetisches Labor und Genetische Beratungsstelle
  • Genetica AG
  • Weinbergstrasse 9
  • 8001 Z▄RICH
  • SWITZERLAND
  • Director of laboratory : Dr Peter ISLER
  • More information
  • Phone : 0041 (0)44 251 90 94
  • Additional Phone : -
  • Fax : 0041 (0)44 261 62 97
  • Website
  • Contact
Last update: September 2019

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
Sanger sequencing

Quality management

EQA
 EQA

EQA scheme(s) organized by EMQN

SCA (Spinocerebellar ataxias)
2014, 2018
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