Nogueira, CéliaVilarinho, LauraPereira, CristinaSilva, LisbethVieira, LuísLeão Teles, ElisaRodrigues, EsmeraldaCampos, TeresaJaneiro, PatriciaCosta, CláudiaGaspar, AnaDupont, JulietteSoares, GabrielaBandeira, AnabelaMartins, EsmeraldaMagalhães, MarinaSantos, Helena2018-04-042018-04-042017-03-18http://hdl.handle.net/10400.18/5530Objectives: The overall aim of our research project was to develop a Next Generation Sequencing strategy to identify nuclear disease causing-mutations in patients suspicious of mitochondrial disorders but without molecular etiology.engMitochondrial DiseasesNGSDoenças Genéticasconference object