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Molecular diagnosis of Autosomal dominant progressive external ophthalmoplegia 5, (RRM2B gene: sequencing of exon 9)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 09/07/2013
  • Neuromuscular Research Unit
  • Department of Neurology
  • University of Tampere
  • ARVO2 building, 3rd floor, room E-318 PO Box 100
  • 33014 UNIVERSITY OF TAMPERE
  • FINLAND
  • Director of laboratory : Pr Bjarne UDD
  • More information
  • Phone : 358 50 318 6286
  • Additional Phone : -
  • Fax : 358 3 364 0557
  • Website
Last update: July 2013

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 genes tested (including panels) (1)

Additional information

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.