Associated Papers
Molecular analysis of gene variants in an Iranian family with psychomotor retardation mitochondrial disorder patient.
Shabannejadian F et al.
Clinical Case Reports, 2023
Emerging Roles of NDUFS8 Located in Mitochondrial Complex I in Different Diseases.
Wang S et al.
Molecules (basel, Switzerland), 2022
Expanding the phenotype of DNAJC30-associated Leigh syndrome.
Zawadzka M et al.
Clinical Genetics, 2022
Cerebral blood flow and acute episodes of Leigh syndrome in neurometabolic disorders.
Loiselet K et al.
Developmental Medicine and Child Neurology, 2021
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