Tbx1, a gene encoded in 22q11.2 copy number variant, is a link between alterations in fimbria myelination and cognitive speed in mice

Copy number variants (CNVs) have provided a reliable entry point to identify the structural correlates of atypical cognitive development. Hemizygous deletion of human chromosome 22q11.2 is associated with impaired cognitive function; however, the mechanisms by which the CNVs contribute to cognitive...

Descripción completa

Detalles Bibliográficos
Autores principales: Hiramoto, Takeshi, Sumiyoshi, Akira, Yamauchi, Takahira, Tanigaki, Kenji, Shi, Qian, Kang, Gina, Ryoke, Rie, Nonaka, Hiroi, Enomoto, Shingo, Izumi, Takeshi, Bhat, Manzoor A., Kawashima, Ryuta, Hiroi, Noboru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054676/
https://www.ncbi.nlm.nih.gov/pubmed/34737458
http://dx.doi.org/10.1038/s41380-021-01318-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054676/
https://www.ncbi.nlm.nih.gov/pubmed/34737458
http://dx.doi.org/10.1038/s41380-021-01318-4

Ejemplares similares