Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause

T E J Theunissen, M Nguyen, R Kamps, AT Hendrickx, S Sallevelt, RWH Gottschalk, CM Calis, APM Stassen, BAE Koning, E N M Mulder-Den Hartog, Kees Schoonderwoerd, SA Fuchs, Y Hilhorst-Hofstee, M Visser, J Vanoevelen, R Szklarczyk, M Gerards, IFM de Coo, D Hellebrekers, HJM Smeets

Research output: Contribution to journalArticleAcademicpeer-review

56 Citations (Scopus)
12 Downloads (Pure)
Original languageUndefined/Unknown
Article number400
JournalFrontiers in Genetics
Publication statusPublished - 2018

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