Leber’s Hereditary Optic Neuropathy from a Rare Variant, m.3700 G > A, in the MT-ND1 Gene in a Family
Makaleler > Tam Makale · 2025
Yazarlar: HÜSEYİN NEZİH ÖZDEMİR, Rana Özerol, Asude DURMAZ, Ayça AYKUT, Neşe ÇELEBİSOY
Neuro-Ophthalmology, Uluslararası, Scopus, 2025, cilt 50, ss 378-380
DOI: 10.1080/01658107.2025.2547404
Özet
Leber’s Hereditary Optic Neuropathy (LHON) is a mitochondrial disease that manifests as severe bilateral vision loss due to the selective degeneration of retinal ganglion cells.1 Although its preva...