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

Genes Dis. 2023 Aug 8;11(4):101071. doi: 10.1016/j.gendis.2023.06.038. eCollection 2024 Jul.

Ramesh K Narayanan^{1

2}, Gonzalo Perez-Siles^{1

2}, Kamila A Marzec³, Alexandra Boyling^{1

2}, Brent Neumann⁴, Manoj P Menezes^{5

6}, Marina L Kennerson^{1

2

7}

¹ Northcott Neuroscience Laboratory, ANZAC Research Institute - Sydney Local Health District, Sydney, NSW 2139, Australia.
² Sydney Medical School, University of Sydney, Sydney, NSW 2050, Australia.
³ ANZAC Research Institute - Sydney Local Health District, Sydney, NSW 2139, Australia.
⁴ Neuroscience Program, Monash Biomedicine Discovery Institute and Department of Anatomy and Developmental Biology, Monash University, Melbourne, Victoria 3800, Australia.
⁵ TY Nelson Department of Neurology and Neurosurgery and Kids Neuroscience, Children's Hospital at Westmead, Westmead, Sydney, NSW 2145, Australia.
⁶ Paediatrics and Child Health, The University of Sydney, Sydney, Sydney, NSW 2145, Australia.
⁷ Molecular Medicine Laboratory, Concord General Repatriation Hospital, Sydney, NSW 2139, Australia.

No abstract available