4.6 Review

Genes for normal sleep and sleep disorders

期刊

ANNALS OF MEDICINE
卷 37, 期 8, 页码 580-589

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/07853890500372047

关键词

apnea; association; circadian; human leucocyte antigen; insomnia; Kleine-Levin syndrome; linkage; narcolepsy; prion protein; sleepwalking; twin

向作者/读者索取更多资源

Sleep and wakefulness are complex behaviors that are influenced by many genetic and environmental factors, which are beginning to be discovered. The contribution of genetic. components to sleep disorders is also increasingly recognized as important. Point mutations in the prion protein, period 2, and the prepro-hypocretin/orexin gene have been found as the cause of a few sleep disorders but the possibility that other gene defects may contribute to the pathophysiology of major sleep disorders is worth in-depth investigations. However, single gene disorders are rare and most common disorders are complex in terms of their genetic susceptibility, environmental effects, gene-gene, and gene-environment interactions. We review here the current progress in the genetics of normal and pathological sleep.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据