Pathogenic SAMD9L variants: Differential diagnosis of CMT and potential pitfall in trio-exome analysisKatja Eggermann,G. Christoph Korenke,Ingo Kurth,Matthias Begemann,Daniela Dey,Cordula KnoppEUROPEAN JOURNAL OF HUMAN GENETICS(2022)引用 0|浏览2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