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机译:在古典Rett综合症和MECP2基因分析患者Rett-like特性。
Department of Human Molecular Genetics, National Public Health Institute, Helsinki, Finland. Mari.Auranen;
nlee.demon.co.uk;
Rett Syndrome; Patients; Methyl-CpG-Binding Protein 2MECP2 geneDNA-Binding Proteinsdevelopmental delay;
机译:基因组学和转录组学分析可以区分经典的Rett和Rett-like综合征,并揭示共享的改变途径。
机译:基因组和转录组学分析可区分经典的Rett和Rett-like综合征并揭示共享的改变途径
机译:肺部缺陷有助于RETT综合征的MECP2 - 突变小鼠模型中的呼吸系统症状
机译:Rett和Rett-like综合征:将基因范围扩展到KIF1A和GRIN1基因
机译:metabolic syndrome is not a predictor for cardiovascular events in Japanese patients with diabetes mellitus asymptomatic for coronary artery disease: a retrospective analysis of the J-aCCEss-2 study