Determinants of sleep disturbances in Rett syndrome: Novel findings in relation to genotype.

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第一作者： Sharolin,Boban

第一单位： Telethon Kids Institute, The University of Western Australia, Perth, Australia.

作者： Sharolin,Boban ^[1] ; Kingsley,Wong ^[1] ; Amy,Epstein ^[1] ; Barbara,Anderson ^[1] ; Nada,Murphy ^[1] ; Jenny,Downs ^[1] ; Helen,Leonard ^[2]

作者单位： Telethon Kids Institute, The University of Western Australia, Perth, Australia. ^[1] School of Physiotherapy and Exercise Science, Curtin University, Perth, Australia. ^[2]

关键词 MECP2 Rett syndrome developmental disability genotype international database rare disorder sleep disorders sleep disturbance scale

主题词青少年(Adolescent);成年人(Adult);儿童(Child);儿童, 学龄前(Child, Preschool);癫痫(Epilepsy);遗传关联研究(Genetic Association Studies);基因型(Genotype);人类(Humans);婴儿(Infant);婴儿, 新生(Infant, Newborn);甲基-CpG-结合蛋白质2(Methyl-CpG-Binding Protein 2);中年人(Middle Aged);突变(Mutation);表型(Phenotype);Rett综合征(Rett Syndrome);疾病严重程度指数(Severity of Illness Index);青年人(Young Adult)

DOI 10.1002/ajmg.a.37784

PMID 27255190

发布时间 2022-04-10

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American journal of medical genetics. Part A

2016年170卷9期

2292-300页

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Determinants of sleep disturbances in Rett syndrome: Novel findings in relation to genotype.

American journal of medical genetics. Part A

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American journal of medical genetics. Part A

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Determinants of sleep disturbances in Rett syndrome: Novel findings in relation to genotype.

American journal of medical genetics. Part A

相似文献

American journal of medical genetics. Part A

相关期刊

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