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作者:Mona Shams Aldeen S
来源:[J].JSM Bioinformatics, Genomics and Proteomics, 2016, Vol.1 (1)
摘要:Severe combined immunodeficiency is an inherited Primary immunodeficiency PID, which is characterized by the absence or dysfunction of T lymphocytes. Defects in RAG1 and RAG2 are known to cause a TBNK+ form of SCID. Recombinase activating genes RAG1 and RAG2 (OMIM 179615,179...

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