Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study

BACKGROUND: Leber hereditary optic neuropathy (LHON) is the most common mitochondrial disorder, frequently resulting in acute or subacute severe bilateral central vision loss. Vitamin B12 deficiency is also a known cause of optic neuropathy through mitochondrial dysfunction. Here we evaluated the pr...

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Detalles Bibliográficos
Autores principales: Zibold, Julia, von Livonius, Bettina, Kolarova, Hana, Rudolph, Günter, Priglinger, Claudia S., Klopstock, Thomas, Catarino, Claudia B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361590/
https://www.ncbi.nlm.nih.gov/pubmed/35945620
http://dx.doi.org/10.1186/s13023-022-02453-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361590/
https://www.ncbi.nlm.nih.gov/pubmed/35945620
http://dx.doi.org/10.1186/s13023-022-02453-z

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