参考文献
妇产科学

        [1] Xu X, Yang X, Wu Q, et al. Amplicon resequencing identified parental mosaicism for approximately 10% of“de novo” SCN1A mutations in children with Dravet syndrome [J]. Hum Mutat, 2015, 36: 861-872.[2] Cetica V, Chiari S, Mei D, et al. Clinical and gene    （共 31555 字）     [阅读本文] >>