Mitochondrial complex I deficiency in a 4-year-old boy due to compound heterozygous NDUFV1 mutation: a case report of a new pathogenic variant

👤 Salim Haddad; Elie Salloum; Abdullah Silan; Gazel kalecioğlu; Maria Abdulnour; Sultaneh Haddad; Diana Alasmar; Mahmoud Alayash; Ahmed Noman Ghaleb 🗓️ 2025

المصدر: Oxford Medical Case Reports · الاستشهادات (Scopus): 2