发现 SLC19A1 基因 rs1051266 变异影响 ASD 临床进程，且患者叶酸代谢标志物变异性大，为个性化防治提供方向。 自闭症谱系障碍（Autism spectrum disorders，ASD）具有临床异质性，且可能与脑叶酸缺乏（Cerebral folate deficiency，CFD）相关。在其病因中，叶酸受体 α 自身抗体 ...

Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children, and can be subcategorized histologically and/or based on PAX-FOXO1 fusion gene status. Over the last four decades, there have ...