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Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations
The purpose of the study is to explore the causative role of TUBB2B gene mutations in patients with different malformations of cortical development. We collected and evaluated clinical and MRI data of a cohort of 128 consecutive patients (61 females and 67 males) in whom brain MRI had detected a spe...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3421113/ https://ncbi.nlm.nih.gov/pubmed/22333901 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.21 |
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