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- Functions of Cytochrome C Oxidase Assembly Factors
- Taysha Gene Therapies Announces Multiple Data Presentations and Workshop Presentations at the 24Th Annual Meeting of the American Society of Gene & Cell Therapy
- Identification of a Novel Deletion in SURF1 Gene
- SURF1 Mutations Causative of Leigh Syndrome Impair Human Neurogenesis
- SURF1 Sequencing Indication
- Mutation Screening in Patients with Isolated Cytochrome C Oxidase Deficiency
- SURF1 Deficiency: a Multi-Centre Natural History Study
- Leigh Syndrome
- Association of Mutations in SCO2, a Cytochrome C Oxidase Assembly Gene, with Early Fetal Lethality
- Leighs Disease: a Rare Case Report
- Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
- And Species-Specific Differences in Cytochrome C Oxidase Assembly
- Genetic Features of Mitochondrial Respiratory Chain Disorders
- Mutation Analysis of COX18 in 29 Patients with Isolated Cytochrome C Oxidase Deficiency
- Monogenic Diseases Masquerading As Multiple Sclerosis
- Sequence Conservation from Human to Prokaryotes of Surf1, a Protein Involved in Cytochrome C Oxidase Assembly, De¢Cient in Leigh Syndrome
- Additional Material 1: SURF1 Study Data Collection Questionnaire
- REVIEW ARTICLE Human Cytochrome Oxidase Deficiency
- Mitochondrial Physiology Network 8.10-A2: 1-29 (2003)
- SURF1 Deficiency
- Functional Alteration of Cytochrome C Oxidase by SURF1 Mutations in Leigh Syndrome
- Inbred Mouse Strains Expression in Primary Immunocytes Across
- Genetic Association of the Cytochrome C Oxidase-Related Genes with Alzheimer’S Disease in Han Chinese
- Novel Mutations in COX15 in a Long Surviving Leigh Syndrome Patient with Cytochrome C Oxidase Deficiency M Bugiani, V Tiranti, L Farina, G Uziel, M Zeviani