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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Detalhes bibliográficos
Publicado no:Genes (Basel)
Main Authors: Dawod, Phepy G. A., Jancic, Jasna, Marjanovic, Ana, Brankovic, Marija, Jankovic, Milena, Samardzic, Janko, Potkonjak, Dario, Djuric, Vesna, Mesaros, Sarlota, Novakovic, Ivana, Abdel Motaleb, Fayda I., Kostic, Vladimir S., Nikolic, Dejan
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7565519/
https://ncbi.nlm.nih.gov/pubmed/32887465
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11091037
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