日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorder

罕见变异的共现表明基因对参与细胞骨架通路,并且与自闭症谱系障碍的严重程度增加有关。

Lee, Hyeji; Ko, Kahee; Kim, Seoyeon; Lee, Ganghee; Kim, Soowhee; Lee, Jihae; Song, Da-Yea; Bong, Guiyoung; Han, Jae Hyun; Lee, Jeewon; Kim, Ye Rim; Lee, Yoojeong; Kim, Eunjoon; Børglum, Anders D; Grove, Jakob; Kim, So Hyun; Sun, Woong; Yoo, Hee Jeong; An, Joon-Yong