Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency [version 2; peer review: 2 approved, 1 not approved]
Govindaraj, Geeta Madathil, Karuthedath Vellarikkal, Shamsudheen, Jayarajan, Rijith, Ravi, Rowmika, Verma, Ankit, Chakkiyar, Krishnan, Jayakrishnan, Machinari Puthenpurayil, Arakkal, Riyaz, Raj, Revathi, Kunnaruvath, Rajeevan, Sivasubbu, Sridhar, Scaria, Vinod
Published in F1000 research (01.01.2016)
Published in F1000 research (01.01.2016)
Get full text
Journal Article
Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency
Govindaraj, Geeta Madathil, Karuthedath Vellarikkal, Shamsudheen, Jayarajan, Rijith, Ravi, Rowmika, Verma, Ankit, Chakkiyar, Krishnan, Jayakrishnan, Machinari Puthenpurayil, Arakkal, Riyaz, Raj, Revathi, Kunnaruvath, Rajeevan, Sivasubbu, Sridhar, Scaria, Vinod
Published in F1000 research (2016)
Published in F1000 research (2016)
Get full text
Journal Article