1 | BLS2D
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| Mutations in the bare lymphocyte syndrome define critical steps in the assembly of the regulatory factor X complex.
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| Nekrep N, Jabrane-Ferrat N, Peterlin BM.
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| Mol Cell Biol 20(12):4455-61. 2000
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2 | BLS2D, RFXAP
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| Genetic and molecular definition of complementation group D in MHC class II deficiency.
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| Fondaneche MC, et al.
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| Hum Mol Genet 7 : 879-885. 1998
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3 | BLS2D, RFX5, RFXAP
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| Mutation of RFXAP, a regulator of MHC class II genes, in primary MHC class II deficiency.
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| Villard J, Lisowska-Grospierre B, van den Elsen P, Fischer A, Reith W, Mach B.
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| N Engl J Med 337(11):748-53. 1997
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4 | BLS2D, RFXAP
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| RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency.
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| Durand B, et al.
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| EMBO J 16 : 1045-1055. 1997
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