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Biallelic mutation of SUPV3L1 causes an inherited leukodystrophy-associated neurodevelopmental disorder due to aberrant mitochondrial double stranded RNA processing

Green, L.; Hamilton, N.; Elpidorou, M.; Harris, E. L.; Douglas, A.; Ounap, K.; Maroofian, R.; Rose, A. M.; Elworthy, S.; Renshaw, S. A.; Low, E. C.; Prescott, T.; Soberg, K.; Al-Maawali, A.; Al-Zuhaib, S.; Al Futaisi, A.; Calame, D.; Al-Thihli, K.; Sheridan, E. G.; Johnson, C. A.; Livingston, J.; Crow, Y. J.; Poulter, J. A.

2023-07-03 neurology
10.1101/2023.07.03.23291502 medRxiv
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Withdrawal StatementThe authors have withdrawn their manuscript owing to an error identified by the corresponding author. Therefore, the authors do not wish this work to be cited as reference for the project. If you have any questions, please contact the corresponding author.

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