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  1. 1
    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]

    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... von 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

    Veröffentlicht in F1000 research

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

    Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency von Govindaraj, Geeta Madathil, Karuthedath Vellarikkal, Shamsudheen, Jayarajan, Rijith, Ravi, Rowmika, Verma, Ankit, Chakkiyar, Krishnan, Jayakrishnan, Machinari Puthenpurayil, Arakkal, Riyaz, Raj, Revathi, Sivasubbu, Sridhar, Scaria, Vinod

    Veröffentlicht in F1000 research

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