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

The ERBB2 c.1795C>T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humans.

ERBB2 c.1795C>T,p.Arg599Cys 变异与人类左心室流出道梗阻缺陷有关

Ampuja Minna, Ericsson Sabina, Paatero Ilkka, Chowdhury Iftekhar, Villman Jenna, Broberg Martin, Ramste Amanda, Balboa Diego, Ojala Tiina, Chong Jessica X, Bamshad Michael J, Priest James R, Varjosalo Markku, Kivelä Riikka, Helle Emmi

Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects

全基因组关联研究揭示了室间隔缺损和左侧先天性心脏缺陷的新风险位点

Broberg, Martin; Ampuja, Minna; Jones, Samuel; Ojala, Tiina; Rahkonen, Otto; Kivelä, Riikka; Priest, James; Palotie, Aarno; Ollila, Hanna M; Helle, Emmi