Orphanet: Diagnosi molecolare della paraplegia spastica geni SPAST, ATL1 e SPG7
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Molecular diagnosis of familial spastic paraplegia (SPAST, ATL1, SPG7 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 27/09/2010
  • Laboratorio di Genetica Molecolare 3
  • Istituto di Scienze Neurologiche
  • CNR
  • Contrada Burga
  • 87050 MANGONE (CS)
  • ITALY
  • Director of laboratory : Dr Maria MUGLIA
  • More information
  • Phone : 39 0984 9801228
  • Additional Phone : -
  • Fax : 39 0984 969306
  • Website
Last update: September 2010

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 diseases tested (1)
List of genes tested (including panels) (3)
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.