Condition: Bare Lymphocyte Syndrome, Type I


rs1222208628 in TAP2 gene and Bare Lymphocyte Syndrome, Type I PMID 23662797 2014 Transporter associated with antigen processing deficiency syndrome: case report of an adolescent with chronic perforated granulomatous skin lesions due to TAP2 mutation.

PMID 11529920 2001 Molecular studies and NK cell function of a new case of TAP2 homozygous human deficiency.

PMID 7517574 1994 Homozygous human TAP peptide transporter mutation in HLA class I deficiency.

PMID 12067308 2002 Asymptomatic deficiency in the peptide transporter associated to antigen processing (TAP).