Congenital defects in a patient carrying a novel homozygous AEBP1 variant could expand the phenotype of Ehlers-Danlos syndrome classical-like type 2Niccolo Di Giosaffatte,Alessandro Ferraris,Federica Gaudioso,Valentina Lodato, Emanuele Savino,Giulia Parise,Filippo Camerota,Claudia Celletti,Simone Bargiacchi,Luigi Laino,Irene Bottillo,Paola GrammaticoEUROPEAN JOURNAL OF HUMAN GENETICS（2023）引用 0|浏览6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
