Omenn syndrome with mutation in RAG1 gene

Indian Journal of Pediatrics

Volumn 75, Issue 9, 2008, Pages 944-946

  Jaouad, I Cherkaoui ^a   Ouldim, K ^a   Ali Ou Alla, S ^b   Kriouile, Y ^b   Villa, A ^c   Sefiani, A ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b IBN SINA HOSPITAL   (Morocco)

^c CNR   (Italy)

Author keywords

Omenn syndrome; RAG; Severe combined immunodeficiency

Indexed keywords

RAG1 PROTEIN;

ARTICLE; CASE REPORT; CLINICAL FEATURE; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC COUNSELING; HUMAN; INFANT; OMENN SYNDROME; POLYMERASE CHAIN REACTION;

ALOPECIA; DERMATITIS, EXFOLIATIVE; DNA-BINDING PROTEINS; FEMALE; GENE REARRANGEMENT, T-LYMPHOCYTE; HEPATOMEGALY; HETEROZYGOTE; HOMEODOMAIN PROTEINS; HUMANS; INFANT; LYMPHATIC DISEASES; MOROCCO; MUTATION; NUCLEAR PROTEINS; SEVERE COMBINED IMMUNODEFICIENCY; SPLENOMEGALY; SYNDROME;

EID: 56349135385     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12098-008-0197-0     Document Type: Article

References (15)

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