TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families

Molecular Genetics and Metabolism 2026

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Authors: Malak Alghamdi, Ahmad Alahmad, Malak Alaboudi, Sulaiman Alsheikh, Mohammed H. Alanazy, Buthaina Albash, Ahmad Alaqeel, Naif A. Almontashiri, Dima Z. Jamjoom, Fahad A. Bashiri, Muddathir H. Hamad, Hebatallah H. Ali
+8 more Mohammed Alwatidi, Essa Alharbi, Sherief Omar, Dana Marafi, Fatima Alabdulrazzaq, Stefan T. Arold, Robert McFarland, Robert W.Taylor
DOI: 10.1016/j.ymgme.2026.109867
Cited by: 2
References: 12

Fields of Study & Subjects

Mitochondrial Function and Pathology Genomics and Rare Diseases ATP Synthase and ATPases Research

Publication details

Journal / source
Molecular Genetics and Metabolism
Publisher
Elsevier BV
Volume
148
Issue
2
Pages
109867–109867
Publication date
9 March 2026
Language
EN