Molecular Analysis of Chinese FOXG1-Related Encephalopathy
<p id="p1">FOXG1-related encephalopathy, also referred to as FOXG1-related disease or FOXG1 syndrome, impacts the majority of developmental elements and results in brain abnormalities and microcephaly. This syndrome was categorized as a congenital variant of Rett syndrome. The primary cause of this...
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| Autores principales: | , , |
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| Formato: | Capítulo de libro |
| Lenguaje: | inglés |
| Publicado: |
IntechOpen
2025
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| Materias: | |
| Acceso en línea: | https://www.intechopen.com/chapters/1225271 |
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