Molecular Screening Reveals De Novo Loss-of-Function NR4A2 Variants in Saudi Children with Autism Spectrum Disorders: A Single-Center Study
分子筛查揭示沙特阿拉伯自闭症谱系障碍儿童中存在新生NR4A2功能缺失变异:一项单中心研究
期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms26125468
Alharbi, Najwa M; Baaboud, Wejdan F; Shawky, Heba; Alrofaidi, Aisha A; Farsi, Reem M; Algothmi, Khloud M; Hassoubah, Shahira A; Basingab, Fatemah S; Azhari, Sheren A; Alharbi, Mona G; Yahya, Reham; Alhazmi, Safiah