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A novel TUBG1 mutation with neurodevelopmental disorder caused by malformations of cortical development
Neurodevelopmental disorder caused by malformations of cortical development is a rare neurological disease. Heterozygous missense variants in the TUBG1 gene lead to malformations of human cortical development, which further result in intellectual disability, developmental retardation, and epilepsy....
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| Publicado no: | Biomed Res Int |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7935588/ https://ncbi.nlm.nih.gov/pubmed/33728335 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2021/6644274 |
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