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Generation and analysis of novel Reln‐deleted mouse model corresponding to exonic Reln deletion in schizophrenia
AIM: A Japanese individual with schizophrenia harboring a novel exonic deletion in RELN was recently identified by genome‐wide copy‐number variation analysis. Thus, the present study aimed to generate and analyze a model mouse to clarify whether Reln deficiency is associated with the pathogenesis of...
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| Pubblicato in: | Psychiatry Clin Neurosci |
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| Autori principali: | , , , , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley & Sons Australia, Ltd
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7318658/ https://ncbi.nlm.nih.gov/pubmed/32065683 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/pcn.12993 |
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