A biallelic gain-of-function variant in MSGN1 causes a new skeletal dysplasia syndrome Asuman Koparir,Caroline Lekszas, Kemal Keseroglu,Aboulfazl Rad,Atefeh Hasanzadeh,Ehsan Ghayoor Karimiani, Nakul Narendran,Ertugrul Ozbudak,Barbara Vona,Thomas HaafEUROPEAN JOURNAL OF HUMAN GENETICS(2023)引用 0|浏览1暂无评分AI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要