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SLC19A1 基因 rs1051266 变异与自闭症谱系障碍及脑叶酸缺乏的关联探秘 ...
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 ...
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