@Article{Rydzanicz2008,
journal="Klinika Oczna / Acta Ophthalmologica Polonica",
issn="0023-2157",
volume="110",
number="3",
year="2008",
title="Mutacje mitochondrialnego DNA w chorobach narządu 
wzroku – dziedziczna neuropatia nerwu wzrokowego 
Lebera oraz zespół Kearnsa",
abstract="Mitochondrial diseases are caused by mitochondrial structure aberrations and function deficiency. The clinical heterogeneity of mitochondrial diseases is associated with the type of causing mutations (de novo or maternally transmitted mutations), and several aspects of mitochondrial genetics and inheritance, including heteroplasmy. In this paper, we explain the basics of mitochondrial genetics and inheritance  as well as genetic background of mitochondrial related disorders: Leber’s hereditary optic neuropathy and Kearns’ syndrome.",
author="Rydzanicz, Małgorzata
and Mrugacz, Małgorzata
and Gajęcka, Marzena",
pages="321--324",
url="https://www.termedia.pl/Mutations-in-mitochondrial-DNA-in-ocular-diseases-r-n-Leber-s-hereditary-optic-neuropathy-and-Kearns-r-nsyndrome,124,48759,1,1.html"
}