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[Not Available].[无可用内容]
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BKca channel in autism and mental retardation.自闭症和智力迟钝中的大电导钙激活钾通道
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Autism and intellectual disability: two sides of the same coin.自闭症与智力残疾：同一硬币的两面。
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Disparate diseases due to copycat copy number variations.由模仿性拷贝数变异导致的不同疾病。
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Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism.Xp22.11 缺失：PTCHD1 是伴或不伴孤独症的 X 连锁智力障碍的候选基因。
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Collybistin binds and inhibits mTORC1 signaling: a potential novel mechanism contributing to intellectual disability and autism.结肠双调蛋白结合并抑制mTORC1信号传导：一种导致智力残疾和自闭症的潜在新机制。
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Association of a functional deficit of the BKCa channel, a synaptic regulator of neuronal excitability, with autism and mental retardation.大电导钙激活钾通道（BKCa通道）是神经元兴奋性的突触调节剂，其功能缺陷与自闭症和智力障碍的关联。
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Genetic and epigenetic networks in intellectual disabilities.智力障碍的遗传和表观遗传网络。
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[Twins with autism and mental retardation associated with balanced (7;20) chromosomal translocation].[患有自闭症和智力障碍且与平衡型（7；20）染色体易位相关的双胞胎]
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Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency.SYNGAP1 基因突变通过诱导杂合子不足导致智力残疾、自闭症和一种特定形式的癫痫。
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