Mitochondrial DNA point mutation in human oocytes is associated with maternal age
- 1 January 2000
- journal article
- Published by Elsevier in Reproductive BioMedicine Online
- Vol. 1 (3) , 96-100
- https://doi.org/10.1016/s1472-6483(10)61946-3
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Mitochondrial DNA heteroplasmy after human ooplasmic transplantationFertility and Sterility, 2000
- Aging-Dependent Large Accumulation of Point Mutations in the Human mtDNA Control Region for ReplicationScience, 1999
- Mitochondrial DNA rearrangements in human oocytes and embryosMolecular Human Reproduction, 1999
- Mitochondrial DNA deletion in human oocytes and embryosMolecular Human Reproduction, 1998
- PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencingNucleic Acids Research, 1997
- Skewed Segregation of the mtDNA nt 8993 (TrG) Mutation in Human OocytesAmerican Journal of Human Genetics, 1997
- Cardiomyopathy with mitochondrial DNA mutationsAmerican Heart Journal, 1991
- Detection of a specific mitochondrial DNA deletion in tissues of older humansNucleic Acids Research, 1990
- Normal oxidative damage to mitochondrial and nuclear DNA is extensive.Proceedings of the National Academy of Sciences, 1988
- Sequence and organization of the human mitochondrial genomeNature, 1981