A Rare m.4171C>A (MT-ND1), p.(Leu289Met) Mutation in Leber’s Hereditary Optic Neuropathy: A Case Series from a Lebanese Armenian Family and a French Patient
Year: 2026
Type: article
Study design: Case Report
Source: Neuro-Ophthalmology
Authors: Sally Al Hassan, Rabih Hage, Alaa Bou Ghannam
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W7172322237