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Case Report: Whole exome sequencing identifies variation c...:
Govindaraj, Geeta Madathil
;
Karuthedath Vellarikkal, Shamsudheen
;
Jayarajan, Rijith
...
F1000Research. 5 (2016) - p. 2532 , 2016
Link:
https://doi.org/10.12688/f1000research.9473.1
RT Journal T1
Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency
UL https://suche.suub.uni-bremen.de/peid=cr-10.12688_f1000research.9473.1&Exemplar=1&LAN=DE A1 Govindaraj, Geeta Madathil A1 Karuthedath Vellarikkal, Shamsudheen A1 Jayarajan, Rijith A1 Ravi, Rowmika A1 Verma, Ankit A1 Chakkiyar, Krishnan A1 Jayakrishnan, Machinari Puthenpurayil A1 Arakkal, Riyaz A1 Raj, Revathi A1 Sivasubbu, Sridhar A1 Scaria, Vinod PB F1000 Research Ltd YR 2016 SN 2046-1402 JF F1000Research VO 5 SP 2532 LK http://dx.doi.org/https://doi.org/10.12688/f1000research.9473.1 DO https://doi.org/10.12688/f1000research.9473.1 SF ELIB - SuUB Bremen
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