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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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Detalhes bibliográficos
Publicado no:Hum Brain Mapp
Main Authors: Cabana, Jean‐François, Gilbert, Guillaume, Létourneau‐Guillon, Laurent, Safi, Dima, Rouleau, Isabelle, Cossette, Patrick, Nguyen, Dang Khoa
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
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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