Orphanet: Diagnosi molecolare dell_atassia spinocerebellare autosomica dominante SCA 1, 2, 3, 6, 7, malattia di Machado Joseph geni ATXN1, ATXN2, ATXN3 e CACNA1A
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Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, Machado-Joseph disease) (ATXN1, ATXN2, ATXN3 and CACNA1A genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 08/10/2010
  • U.O.C. di Medicina Molecolare
  • Dipartimento dei Servizi
  • Azienda Ospedaliera Universitaria Senese - Ospedale Santa Maria alle Scotte
  • Viale Mario Bracci
  • 53100 SIENA
  • ITALY
  • Director of laboratory : Pr Vincenzo SORRENTINO
  • More information
  • Phone : 39 0577 234192
  • Additional Phone : 39 0577 586261
  • Fax : 39 0577 234191
  • Website
  • Contact
Last update: October 2010

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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