Orphanet: Diagn�stico molecular da dem�ncia fronto temporal genes MAPT, PGRN, VCP e CHMP2B: sequencia��o de toda a regi�o codificante.

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Molecular diagnosis of frontotemporal dementia (MAPT, PGRN, VCP and CHMP2B genes): sequencing of the entire coding region.

Despite our efforts to ensure that data is up to date, this activity has not been validated since 15/04/2015
  • GENOMED, Diagnsticos de Medicina Molecular
  • Instituto de Medicina Molecular - Faculdade de Medicina da Universidade de Lisboa
  • Faculdade de Medicina da Universidade de Lisboa
  • Av. Professor Egas Moniz
  • 1649-028 LISBOA
  • Director of laboratory : Dr Teresa C PORTA NOVA
  • More information
  • Phone : 351 217 999 501
  • Additional Phone : -
  • Fax : 351 217 999 500
  • Website
  • Contact
Last update: April 2015

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (4)
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