Search for a diagnostic test
Molecular diagnosis of Dementia (NGS panel for MAPT, PGRN, VCP, PRNP, SCNA, SNCB, CHMP2B, FUS, TARDBP, PSEN1, PSEN2, APOE, APP 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 31/07/2014- Centro de Genética Preditiva e Preventiva - IBMC
- Instituto de Biologia Molecular e Celular
- Rua do Campo Alegre, 823
- 4150-180 PORTO
- PORTUGAL
- Director of laboratory : Pr Jorge SEQUEIROS
- More information
Last update: July 2014
Responsible of diagnostic test
Purpose(s)
Post-natal diagnosis
Technical procedure(s)
Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)
List of diseases and genes
List of diseases tested
(17)
Additional information
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.