C. elegans model of riboflavin transporter deficiency (RTD) disorder reveals deficits in synaptic transmission and movement

• Ramesh K. Narayanan,
• Gonzalo Perez-siles,
• Kamila A. Marzec,
• Alexandra Boyling,
• Brent Neumann,
• Manoj P. Menezes,
• Marina L. Kennerson

Affiliations

Ramesh K. Narayanan

Northcott Neuroscience Laboratory, ANZAC Research Institute - Sydney Local Health District, Sydney, NSW 2139, Australia; Sydney Medical School, University of Sydney, Sydney, NSW 2050, Australia; Corresponding author. Northcott Neuroscience Laboratory, ANZAC Research Institute - Sydney Local Health District, Sydney, NSW 2139, Australia.

Gonzalo Perez-siles

Northcott Neuroscience Laboratory, ANZAC Research Institute - Sydney Local Health District, Sydney, NSW 2139, Australia; Sydney Medical School, University of Sydney, Sydney, NSW 2050, Australia

Kamila A. Marzec

ANZAC Research Institute - Sydney Local Health District, Sydney, NSW 2139, Australia

Alexandra Boyling

Northcott Neuroscience Laboratory, ANZAC Research Institute - Sydney Local Health District, Sydney, NSW 2139, Australia; Sydney Medical School, University of Sydney, Sydney, NSW 2050, Australia

Brent Neumann

Neuroscience Program, Monash Biomedicine Discovery Institute and Department of Anatomy and Developmental Biology, Monash University, Melbourne, Victoria 3800, Australia

Manoj P. Menezes

TY Nelson Department of Neurology and Neurosurgery and Kids Neuroscience, Children's Hospital at Westmead, Westmead, Sydney, NSW 2145, Australia; Paediatrics and Child Health, The University of Sydney, Sydney, Sydney, NSW 2145, Australia

Marina L. Kennerson

Northcott Neuroscience Laboratory, ANZAC Research Institute - Sydney Local Health District, Sydney, NSW 2139, Australia; Sydney Medical School, University of Sydney, Sydney, NSW 2050, Australia; Molecular Medicine Laboratory, Concord General Repatriation Hospital, Sydney, NSW 2139, Australia