A Novel Congenital Disorder of Glycosylation, AGM1-CDG, with T-B-NK plus SCID, Neutropenia and Skeletal Dysplasia, Caused by Mutations in the Gene Encoding Phosphoacetylglucosamine Mutase 1
JOURNAL OF CLINICAL IMMUNOLOGY(2014)
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