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Effects of SYN1(Q555X) mutation on cortical gray matter microstructure
A new Q555X mutation on the SYN1 gene was recently found in several members of a family segregating dyslexia, epilepsy, and autism spectrum disorder. To describe the effects of this mutation on cortical gray matter microstructure, we performed a surface‐based group study using novel diffusion and qu...
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| Publicado no: | Hum Brain Mapp |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6866302/ https://ncbi.nlm.nih.gov/pubmed/29671924 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hbm.24186 |
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