(Q3508735)

English

Bare lymphocyte syndrome

medical condition

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Statements

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2 references

Combined immunodeficiency disease associated with absence of cell-surface HLA-A and -B antigens

Defective expression of HLA class I antigens: a case of the bare lymphocyte without immunodeficiency.

severe combined immunodeficiency

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health specialty

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genetic association

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A trans-acting class II regulatory gene unlinked to the MHC controls expression of HLA class II genes

Mutation in a winged-helix DNA-binding motif causes atypical bare lymphocyte syndrome

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A trans-acting class II regulatory gene unlinked to the MHC controls expression of HLA class II genes

Mutation in a winged-helix DNA-binding motif causes atypical bare lymphocyte syndrome

1 reference

Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHC class II deficiency

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Homozygous human TAP peptide transporter mutation in HLA class I deficiency

Identifiers

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imported from Wikimedia project

English Wikipedia

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imported from Wikimedia project

English Wikipedia

GARD rare disease ID

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imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

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imported from Wikimedia project

English Wikipedia

1 reference

imported from Wikimedia project

English Wikipedia

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