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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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| Publicado no: | Mol Brain |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6864969/ https://ncbi.nlm.nih.gov/pubmed/31747920 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-019-0519-3 |
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