Orphanet: Molecular diagnosis of Spinocerebellar Ataxia type 7 ATXN7 gene

Search for a diagnostic test

* (*) mandatory field

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 10/05/2011
  • Cheshire & Merseyside Regional Genetics Laboratory Services - Molecular Genetics
  • Liverpool Women's NHS Foundation Trust
  • Crown Street
  • Director of laboratory : Dr Emma HOWARD
  • More information
  • Phone : 44 (0)151 702 4228
  • Additional Phone : -
  • Fax : 44 (0)151 702 4226
  • Website
Last update: May 2011

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics

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.