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

NAA10 p.(N101K) disrupts N-terminal acetyltransferase complex NatA and is associated with developmental delay and hemihypertrophy

NAA10 p.(N101K)会破坏 N 端乙酰转移酶复合物 NatA,并与发育迟缓和半肥大有关

Nina McTiernan, Harinder Gill, Carlos E Prada, Harry Pachajoa, Juliana Lores; CAUSES study; Thomas Arnesen0

Shortened consent forms for genome-wide sequencing: Parent and provider perspectives

基因组测序知情同意书的简化版:家长和医护人员的视角

Hitchcock, Emma C; Study, Causes; Elliott, Alison M

Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy

KCNQ5 的功能丧失和功能获得突变导致智力障碍或癫痫性脑病

Anna Lehman, Samrat Thouta, Grazia M S Mancini, Sakkubai Naidu, Marjon van Slegtenhorst, Kirsty McWalter, Richard Person, Jill Mwenifumbo, Ramona Salvarinova; CAUSES Study; EPGEN Study; Ilaria Guella, Marna B McKenzie, Anita Datta, Mary B Connolly, Somayeh Mojard Kalkhoran, Damon Poburko, Jan M Frie