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Variant recurrence confirms the existence of a FBXO31‐related spastic‐dystonic cerebral palsy syndrome
The role of genetics in the causation of cerebral palsy has become the focus of many studies aiming to unravel the heterogeneous etiology behind this frequent neurodevelopmental disorder. A recent paper reported two unrelated children with a clinical diagnosis of cerebral palsy, who carried the same...
| Autores principales: | , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8045898/ https://www.ncbi.nlm.nih.gov/pubmed/33675180 http://dx.doi.org/10.1002/acn3.51335 |