نتایج جستجو برای: heteroplasmy

تعداد نتایج: 700  

Journal: :Journal of applied genetics 2003
Katarzyna Mroczek-Tońska Bartłomiej Kisiel Janusz Piechota Ewa Bartnik

Leber hereditary optic neuropathy is a maternally inherited type of blindness caused by degeneration of the optic nerve. It is caused by point mutations in mitochondrial DNA. Like in other mitochondrial diseases, its penetrance and inheritance is complicated by heteroplasmy, tissue distribution, and the bottleneck phenomenon in oocyte maturation. On the cellular level, the mechanism of the dise...

Journal: :Molecular Genetics and Metabolism Reports 2017

Journal: :Forensic Science International-genetics 2021

Nuclear mitochondrial DNA (mtDNA) segments (NUMTs) were discovered shortly after sequencing the first human genome. They have earlier been considered to represent archaic elements of ancient insertion events, but modern technologies and growing databases mtDNA NUMT sequences confirm that they are abundant some them phylogenetically young. Here, we build upon mtDNA/NUMT review articles published...

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