Orphanet: Molecular diagnosis of Amyloidosis, Finnish type Gelsolin gene GSN: specific mutation analysis

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Molecular diagnosis of Amyloidosis, Finnish type (Gelsolin gene (GSN): specific mutation analysis)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 13/01/2012
  • Wessex Regional Genetics Laboratory
  • Salisbury District Hospital
  • Odstock Road
  • Director of laboratory : Dr John CK BARBER
  • More information
  • Phone : 44 (0)1722 429 080
  • Additional Phone : -
  • Fax : 44 (0)1722 338 095
  • Website
Last update: January 2012

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)
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