Orphanet: Diagnosi molecolare della sordit� non sindromica legata alla connessina 26 geni GJB2, GJB6

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Molecular diagnosis of non syndromic deafness due to connexin 26 anomaly (GJB2, GJB6 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 14/09/2011
  • U.O. di Neurogenetica Molecolare
  • Dipartimento di Diagnostica e Tecnologia Applicata
  • Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
  • Via Libero Temolo 4
  • 20126 MILANO
  • Director of laboratory : Dr Barbara GARAVAGLIA
  • More information
  • Phone : 39 02 23942604
  • Additional Phone : 39 02 23942618
  • Fax : 39 02 23942619
  • Website
  • Contact
Last update: September 2011

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics

List of diseases and genes

List of genes tested (including panels) (2)
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