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Oxidative stress, serotonergic changes and decreased ultrasonic vocalizations in a mouse model of Smith Lemli Opitz Syndrome
Smith Lemli Opitz syndrome is an inherited monogenic disorder in which mutations to the Dhcr7 gene lead to deficits in cholesterol synthesis. As a result, many patients suffer from gross physiological and neurological deficits. The purpose of this study was to identify a potential abnormal behaviora...
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| 發表在: | Genes Brain Behav |
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| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5495606/ https://ncbi.nlm.nih.gov/pubmed/28220990 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/gbb.12376 |
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