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Updated: Jun 7, 2025

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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伊朗人群中自闭症谱系障碍中Csnk1a1p的改变表达:病例控制研究

Zahra Rahmani1, Dina Rahmani1, Marie Saghaeian Jazi2

  • 1Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Scientific reports
|November 16, 2024
PubMed
概括

这项研究发现,自闭症谱系障碍 (ASD) 儿童的Csnk1a1p长非编码RNA水平较低. Csnk1a1p显示出作为ASD诊断生物标志物的潜力.

关键词:
自闭症谱系障碍 自闭症谱系障碍在Csnk1a1p.在 DISC2 中使用 DISC2.在 Evf2 中使用.狐g1-as1 的意思林克 (Linc0094545) 公司

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