HIGHLIGHTS
- who: Report et al. from the Pediatrics, Saudi German Hospital Jeddah, Jeddah, Medicine, King Abdulaziz University Hospital, Jeddah have published the research: Review began 09/28/2022 Review ended 10/14/2022 Published 10/22/2022 u00a9 Copyright, in the Journal: (JOURNAL) of October/22,/2022
- what: The authors report the first case of a heterogeneous mutation in both SCN2A and PUM1 genes occurring in a pediatric patient.
- future: The authors desire further studies to be conducted in the near future providing definitive treatment for such patients to improve their quality of life . . .
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