المؤلفون: Wim Trypsteen, Filip Van Nieuwerburgh, Ward De Spiegelaere, Björn Heindryckx, Willem van Snippenberg, Mao-Xing Tang, Yannick Gansemans, Olivier Tytgat, Sofie Symoens, Ramesh Reddy Guggilla, Annekatrien Boel, Michiel Van Herp, Dieter Deforce, Paul Coucke

المصدر: Clinical Chemistry. 67:968-976

مصطلحات موضوعية: 0301 basic medicine, Genetics, Mutation rate, Mitochondrial DNA, 030219 obstetrics & reproductive medicine, Mitochondrial disease, Biochemistry (medical), Clinical Biochemistry, Leber's hereditary optic neuropathy, High-Throughput Nucleotide Sequencing, Fertilization in Vitro, Biology, medicine.disease, DNA, Mitochondrial, Polymerase Chain Reaction, Heteroplasmy, Minor allele frequency, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Mutation, Mutation (genetic algorithm), medicine, Humans, Digital polymerase chain reaction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e712fc0adee6b0919baa49f4d08e97b
https://doi.org/10.1093/clinchem/hvab021