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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...

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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

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