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Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2
A. Reghan Foley, Manoj P. Menezes, Amelie Pandraud, Michael A. Gonzalez, Ahmad Al-Odaib, Alexander J. Abrams, Kumiko Sugano, Atsushi Yonezawa, Adnan Y. Manzur, Joshua Burns, Imelda Hughes, B. Gary McCullagh, Heinz Jungbluth, Ming J. Lim, Jean-Pierre Lin, Andre Megarbane, J. Andoni Urtizberea, Ayaz H. Shah, Jayne Antony, Richard Webster
*Corresponding author for this work
- University of Sydney
- Kyoto University
- Royal Manchester Children's Hospital
- St Thomas Hosp, Guy's & St Thomas' NHS Foundation Trust, Evelina Childrens Hosp, Dept Paediat Neurol
- Saint Joseph University Beirut
- Hop Marin de Hendaye, AP HP
- Great Ormond Street Hospital for Children NHS Trust
- Childrens Univ Hosp, Dept Paediat Neurol
- Sheffield Children's NHS Foundation Trust, Sheffield Children's Hospital
- Childrens Hosp, Children's Medical Research Institute - Australia, Dept Audiol
- Royal Prince Alfred Hosp, Inst Clin Neurosci
- Newcastle University
- Beaumont Hosp, Dept Pathol
- University of Pennsylvania
- University College London
- Miami University
- Childrens Hosp Westmead, Children's Medical Research Institute - Australia, Inst Neurosci & Muscle Res
Research output: Contribution to journal › Article › peer-review
130
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