Orphanet: Molecular diagnosis of Erythrokeratodermia variabilis: complete sequencing of GJB3 Cx 31 and GJB4 Cx 30.3 genes
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Molecular diagnosis of Erythrokeratodermia variabilis: complete sequencing of GJB3 (Cx 31) and GJB4 (Cx 30.3) genes

Despite our efforts to ensure that data is up to date, this activity has not been validated since 12/10/2007
  • Laboratory of Cutaneous Biology
  • Dermatology and venereology Unit
  • Centre Hospitalier Universitaire Vaudois CHUV - Hôpital Beaumont -
  • Avenue de Beaumont 29
  • 1011 LAUSANNE
  • SWITZERLAND
  • Director of laboratory : -
  • More information
  • Phone : 0041 (0)21 314 03 60
  • Additional Phone : -
  • Fax : 0041 (0)21 314 03 82
  • Website
Last update: October 2007

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
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List of diseases and genes

List of diseases tested (1)
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.