Orphanet: Diagnosi molecolare della miopatia nemalinica gene ACTA1
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Molecular diagnosis of nemalinic myopathy (ACTA1 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 18/11/2011
  • U.O. Neurologia IV - Malattie Neuromuscolari e Neuroimmunologia
  • Diagnostica Genetico Molecolare e Neuroimmunologica delle Malattie Neuromuscolari
  • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
  • Via Celoria 11
  • 20133 MILANO MI
  • ITALY
  • Director of laboratory : Dr Pia BERNASCONI
  • More information
  • Phone : 39 02 23942255
  • Additional Phone : -
  • Fax : 39 02 70633874
  • Website
  • Contact
Last update: November 2011

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 genes tested (including panels) (1)
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