Correlation between GLA rare variants and phenotype in Hungarian patients with Fabry diseaseSzlepak Tamas,Sepp Robert,Rakoczi Eva,Nemeth Krisztina, Gyimesi Tamas,Molnar Sandor,Fekete Gyorgy, Judit Molnar MariaEUROPEAN 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