Autism-like behaviors in male mice with a Pcdh19 deletion

Mutations in protocadherin 19 (PCDH19), which is on the X-chromosome, cause the brain disease Epilepsy in Females with Mental Retardation (EFMR). EFMR is also often associated with autism-like symptoms. In mice and humans, epilepsy occurs only in heterozygous females who have a mixture of PCDH19 wil...

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Detalles Bibliográficos
Autores principales: Lim, Jisoo, Ryu, Jiin, Kang, Shinwon, Noh, Hyun Jong, Kim, Chul Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Micro Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864969/
https://www.ncbi.nlm.nih.gov/pubmed/31747920
http://dx.doi.org/10.1186/s13041-019-0519-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864969/
https://www.ncbi.nlm.nih.gov/pubmed/31747920
http://dx.doi.org/10.1186/s13041-019-0519-3

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