P191: Mitochondrial dysfunction in Rett syndrome: Searching for biomarkers

• Ashley Hertzog,
• Adviye Ayper Tolun,
• Carolyn Ellaway,
• Wendy Gold,
• Gladys Ho

Affiliations

Ashley Hertzog

NSW Biochemical Genetics Service, The Children’s Hospital at Westmead, Sydney, NSW, Australia; Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia; Molecular Neurobiology Research Laboratory, Kids Research, Children's Hospital at Westmead, and Children's Medical Research Institute, Westmead, NSW, Australia

Adviye Ayper Tolun

NSW Biochemical Genetics Service, The Children’s Hospital at Westmead, Sydney, NSW, Australia; Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia

Carolyn Ellaway

Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia; Genetic Metabolic Disorders Service, Sydney Children’s Hospitals Network, Sydney, NSW, Australia

Wendy Gold

Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia; Molecular Neurobiology Research Laboratory, Kids Research, Children's Hospital at Westmead, and Children's Medical Research Institute, Westmead, NSW, Australia; Kids Neuroscience Centre, Kids Research, Children's Hospital at Westmead, Westmead, NSW, Australia

Gladys Ho

Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia; Department of Molecular Genetics, Sydney Genome Diagnostics, The Children's Hospital at Westmead, Westmead, NSW, Australia