Orphanet: Molecular diagnosis of Spinocerebellar Ataxia type 7 ATXN7 gene
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Molecular diagnosis of Spinocerebellar Ataxia type 7 (ATXN7 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 18/05/2011
  • East Anglian Medical Genetics Service - Molecular genetics laboratory
  • Box 143
  • Addenbrooke's Hospital
  • Hills Road
  • CAMBRIDGE CB2 0QQ
  • UNITED KINGDOM
  • Director of laboratory : Dr Stephen ABBS
  • More information
  • Phone : 44 (0)1223 348 866
  • Additional Phone : -
  • Fax : 44 (0)1223 348 870
  • Website
  • Contact
Last update: May 2011

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (1)
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.