Mice with mutations in Trpm1, a gene in the locus of 15q13.3 microdeletion syndrome, display pronounced hyperactivity and decreased anxiety-like behavior

The 15q13.3 microdeletion syndrome is a genetic disorder characterized by a wide spectrum of psychiatric disorders that is caused by the deletion of a region containing 7 genes on chromosome 15 (MTMR10, FAN1, TRPM1, MIR211, KLF13, OTUD7A, and CHRNA7). The contribution of each gene in this syndrome h...

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Detalles Bibliográficos
Autores principales: Hori, Tesshu, Ikuta, Shohei, Hattori, Satoko, Takao, Keizo, Miyakawa, Tsuyoshi, Koike, Chieko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008678/
https://www.ncbi.nlm.nih.gov/pubmed/33785025
http://dx.doi.org/10.1186/s13041-021-00749-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008678/
https://www.ncbi.nlm.nih.gov/pubmed/33785025
http://dx.doi.org/10.1186/s13041-021-00749-y

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