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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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Genes Brain Behav
Prif Awduron: Sharif, Navila F, Korade, Zeljka, Porter, Ned A, Harrison, Fiona E
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2017
Pynciau:
Mynediad Ar-lein: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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