Orphanet: Molecular diagnosis of spinocerebellar ataxia 1, 2, 3, 6 and 7 ATXN1, ATXN2, ATXN3, CACNA1A and ATXN7 genes
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Molecular diagnosis of spinocerebellar ataxia 1, 2, 3, 6 and 7 (ATXN1, ATXN2, ATXN3, CACNA1A and ATXN7 genes)

  • Avdeling for medisinsk genetikk
  • Haukeland University Hospital
  • Jonas Liesvei 65
  • 5021 BERGEN
  • NORWAY
  • Director of laboratory : Pr Gunnar HOUGE
  • More information
  • Phone : 47 55 97 54 76
  • Additional Phone : -
  • Fax : 47 55 97 54 79
  • Website
  • Contact
Last update: August 2019

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
PCR based techniques
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