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Molecular diagnosis of Familial Cardiac Conduction Defect (SCN5A and TRPM4 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 15/05/2012
  • Phone : +31 (0)20 566 5110
  • Additional Phone : -
  • Fax : +31 (0)20 566 9389
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Last update: May 2012

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of genes tested (including panels) (2)
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.