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Doublecortin Mutation in an Adolescent Male
Doublecortin (DCX) mutations cause abnormal development of the DCX protein that normally aids in neuronal migration during fetal development. These mutations lead to lissencephaly, or the appearance of a “smooth brain,” which is varying levels of pachygyria or agyria in severe cases. Many genetic va...
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| Publicado no: | Child Neurol Open |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6591519/ https://ncbi.nlm.nih.gov/pubmed/31259193 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2329048X19836589 |
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