A novel pathogenic mutation on Interleukin-7 receptor leading to severe combined immunodeficiency identified with newborn screening and whole exome sequencing

研究成果: Article同行評審

8 引文 斯高帕斯(Scopus)

指紋

深入研究「A novel pathogenic mutation on Interleukin-7 receptor leading to severe combined immunodeficiency identified with newborn screening and whole exome sequencing」主題。共同形成了獨特的指紋。

Medicine & Life Sciences