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A SNP in the ABCC11 gene is the determinant of human earwax type.
Nat Genet. 2006 Mar;38(3):324-30. doi: 10.1038/ng1733. Epub 2006 Jan 29.
Nat Genet. 2006.
PMID: 16444273
RFX-B is the gene responsible for the most common cause of the bare lymphocyte syndrome, an MHC class II immunodeficiency.
Nagarajan UM, Louis-Plence P, DeSandro A, Nilsen R, Bushey A, Boss JM.
Nagarajan UM, et al.
Immunity. 1999 Feb;10(2):153-62. doi: 10.1016/s1074-7613(00)80016-3.
Immunity. 1999.
PMID: 10072068
Free article.
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A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients.
Masternak K, Barras E, Zufferey M, Conrad B, Corthals G, Aebersold R, Sanchez JC, Hochstrasser DF, Mach B, Reith W.
Masternak K, et al.
Nat Genet. 1998 Nov;20(3):273-7. doi: 10.1038/3081.
Nat Genet. 1998.
PMID: 9806546
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