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lüll TAP deficiency syndrome Gadola SD; Moins-Teisserenc HT; Trowsdale J; Gross WL; Cerundolo VClin Exp Immunol 2000[Aug]; 121 (2): 173-8ä|ATP Binding Cassette Transporter, Subfamily B, Member 2[MESH]|ATP Binding Cassette Transporter, Subfamily B, Member 3[MESH]|ATP-Binding Cassette Transporters/chemistry/genetics/*physiology[MESH]|Antigen Presentation[MESH]|Biological Transport[MESH]|Bronchiectasis/etiology[MESH]|Child[MESH]|Child, Preschool[MESH]|Diagnosis, Differential[MESH]|Dimerization[MESH]|Genetic Predisposition to Disease[MESH]|Granuloma/etiology/pathology[MESH]|HLA Antigens/immunology/metabolism[MESH]|Humans[MESH]|Immunocompromised Host[MESH]|Immunologic Deficiency Syndromes/diagnosis[MESH]|Immunosuppressive Agents/therapeutic use[MESH]|Infant[MESH]|Infections/etiology[MESH]|Interferons/therapeutic use[MESH]|Major Histocompatibility Complex[MESH]|Necrosis[MESH]|Phenotype[MESH]|Photochemotherapy[MESH]|Sarcoidosis/diagnosis[MESH]|Severe Combined Immunodeficiency/classification/diagnosis/*genetics/immunology/therapy[MESH]|Skin Diseases/etiology/pathology[MESH]|Skin Ulcer/etiology/therapy[MESH]|Syndrome[MESH] |