Cardiac conduction abnormalities in Leber Hereditary Optic Neuropathy and asymptomatic maternal relatives

Eye (Lond). 2023 Oct;37(14):3050-3051. doi: 10.1038/s41433-023-02466-3. Epub 2023 Mar 6.

Authors

Clare Quigley¹, Glynis Hanrahan², Kirk Stephenson², Saba Ahmed³, Muhammad Mukhtar³, Lorraine Cassidy²

Affiliations

¹ Department of Ophthalmology, Royal Victoria Eye and Ear Hospital, Adelaide Road, Dublin, D02 XK51, Ireland. quigleyclare@gmail.com.
² Department of Ophthalmology, Royal Victoria Eye and Ear Hospital, Adelaide Road, Dublin, D02 XK51, Ireland.
³ Department of Anaesthetics, Royal Victoria Eye and Ear Hospital, Adelaide Road, Dublin, D02 XK51, Ireland.

PMID: 36879160
PMCID: PMC10517109 (available on 2024-10-01)
DOI: 10.1038/s41433-023-02466-3

No abstract available

Publication types

Letter

MeSH terms

DNA, Mitochondrial / genetics
Humans
Mutation
Optic Atrophy, Hereditary, Leber* / genetics

Substances

DNA, Mitochondrial