A novel mutation for TAP deficiency and its possible association with Toxoplasmosis

Parasitology International

Volumn 55, Issue 3, 2006, Pages 219-222

  Doǧu, Figen ^a   Ikincioǧullari, Aydan ^a   Fricker, Dominique ^b   Bozdoǧan, Günseli ^a   Aytekin, Caner ^a   Ileri, Meltem ^a   Teziç, Tahsin ^c   Babacan, Emel ^a   De La Salle, Henri ^b  

^a ANKARA UNIVERSITY   (Turkey)

^b INSERM   (France)

^c DR SAMI ULUS CHILDREN S HOSPITAL   (Turkey)

Author keywords

Granuloma; HLA Class I deficiency; TAP deficiency; Therapy; Toxoplasmosis

Indexed keywords

AMPHOTERICIN B LIPID COMPLEX; CARRIER PROTEIN; COTRIMOXAZOLE; FANSIDAR; FOLIC ACID; IMIPENEM; IMMUNOGLOBULIN; TEICOPLANIN; TRANSPORTER ASSOCIATED TO ANTIGEN PROCESSING; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ANTIBIOTIC THERAPY; ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; FEMALE; GENE MUTATION; HLA ANTIGEN CLASS 1 DEFICIENCY; HUMAN; IMMUNOPATHOLOGY; LUNG INFECTION; MALE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RECURRENT INFECTION; SKIN GRANULOMA; TOXOPLASMOSIS; TREATMENT OUTCOME;

ADULT; ATP-BINDING CASSETTE TRANSPORTERS; B-LYMPHOCYTES; CHILD; CODON, NONSENSE; CONSANGUINITY; FEMALE; GENES, MHC CLASS I; HUMANS; IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; LEUKOCYTES, MONONUCLEAR; MALE; POINT MUTATION; TOXOPLASMOSIS;

EID: 33745884080     PISSN: 13835769     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.parint.2006.02.003     Document Type: Article

References (10)

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