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VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report
BACKGROUND: The mitochondrial respiratory chain defects have become the most common cause of neurometabolic disorders in children and adults, which can occur at any time in life, often associated with neurological dysfunction, and lead to chronic disability and premature death. Approximately one-thi...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Baishideng Publishing Group Inc
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453344/ https://www.ncbi.nlm.nih.gov/pubmed/36157797 http://dx.doi.org/10.12998/wjcc.v10.i24.8749 |