Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy

Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy

Leber’s hereditary optic neuropathy (LHON) is a maternally inherited disorder that affects central vision in young adults and is typically associated with mitochondrial DNA (mtDNA) mutations. This study is based on a mutational screening of entire mtDNA in eight Serbian probands clinically and genet...

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Bibliographic Details
Main Authors: Phepy G. A. Dawod, Jasna Jancic, Ana Marjanovic, Marija Brankovic, Milena Jankovic, Janko Samardzic, Dario Potkonjak, Vesna Djuric, Sarlota Mesaros, Ivana Novakovic, Fayda I. Abdel Motaleb, Vladimir S. Kostic, Dejan Nikolic
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Genes
Subjects:
Leber’s hereditary optic neuropathy
mtDNA
mutations
haplogroups
Online Access:https://www.mdpi.com/2073-4425/11/9/1037

Internet

https://www.mdpi.com/2073-4425/11/9/1037

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