Clinical expression and mitochondrial deoxyribonucleic acid study in twins with 14484 Leber’s hereditary optic neuropathy: A case report

BACKGROUND: This study aimed to explore clinical and molecular factors that cause discordance for clinical expression of Leber’s hereditary optic neuropathy (LHON) in a pair of identical twins with the 14484 point mutation. CASE SUMMARY: Twin patients with the 14484 point mutation were studied for z...

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Detalles Bibliográficos
Autores principales: Chuenkongkaew, Wanicha Leetiratanai, Chinkulkitnivat, Buakhwan, Lertrit, Patcharee, Chirapapaisan, Niphon, Kaewsutthi, Supannee, Suktitipat, Bhoom, Mitrpant, Chalermchai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297404/
https://www.ncbi.nlm.nih.gov/pubmed/36051150
http://dx.doi.org/10.12998/wjcc.v10.i20.6944

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297404/
https://www.ncbi.nlm.nih.gov/pubmed/36051150
http://dx.doi.org/10.12998/wjcc.v10.i20.6944

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