The case of the bare lymphocyte syndrome--tracking down faulty transcription factors
- PMID: 9287236
- DOI: 10.1056/NEJM199709113371110
The case of the bare lymphocyte syndrome--tracking down faulty transcription factors
Comment on
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Mutation of RFXAP, a regulator of MHC class II genes, in primary MHC class II deficiency.N Engl J Med. 1997 Sep 11;337(11):748-53. doi: 10.1056/NEJM199709113371104. N Engl J Med. 1997. PMID: 9287230
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