A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypesLeo Kager,Raul Jimenez-Heredia,Petra Zeitlhofer,Wolfgang Novak,Sebastian K. Eder,Anna Segarra-Roca,Alexandra Frohne,Karin Nebral,Matthias Haimel,Rene Geyeregger, Katharina Roetzer-Londgin,Oskar A. Haas,Kaan BoztugHEMASPHERE（2024）引用 0|浏览17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
