دورية أكاديمية

Novel compound heterozygous mutations in the AFG3L2 gene in a Chinese child with microcephaly, early-onset seizures, and cerebral atrophy

التفاصيل البيبلوغرافية
العنوان: Novel compound heterozygous mutations in the AFG3L2 gene in a Chinese child with microcephaly, early-onset seizures, and cerebral atrophy
المؤلفون: Jin, Tingting, Kuang, Ying, Luo, Shulin, Wang, Rongpin, Chen, Kun, Jiang, Minmin, Ren, Lingyan, Sun, Zhaolin, Duan, Lifen, Huang, Shengwen
المصدر: In Heliyon April 2023 9(4)
قاعدة البيانات: ScienceDirect
الوصف
تدمد:24058440
DOI:10.1016/j.heliyon.2023.e14766