论文信息 - Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency - 字舞流文

Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency

V. Scaria | S. Sivasubbu | A. Verma | R. Jayarajan | Revathi Raj | G. Govindaraj | M. Jayakrishnan | Riyaz Arakkal | S. Karuthedath Vellarikkal | R. Ravi | Krishnan Chakkiyar | Rajeevan Kunnaruvath