WHOLE-EXOME SEQUENCING FOR IDENTIFICATION OF A POTENTIAL NOVEL DEFECT IN A PATIENT WITH RAPID-ONSET FATAL VIRUS-ASSOCIATED HEMOPHAGOCYTIC SYNDROME (VAHS)

JOURNAL OF CLINICAL IMMUNOLOGY(2012)

引用 0|浏览10
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