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