Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a coronin-1A mutation and a chromosome 16p11.2 deletion

Clinical Immunology

Volumn 131, Issue 1, 2009, Pages 24-30

  Shiow, Lawrence R ^b   Paris, Kenneth ^c   Akana, Matthew C ^a   Cyster, Jason G ^a,b   Sorensen, Ricardo U ^c   Puck, Jennifer M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Actin cytoskeleton; Attention deficit and hyperactivity; Autism spectrum; Chromosome 16p11.2; Coronin 1A; SCID

Indexed keywords

ACICLOVIR; ALEMTUZUMAB; CHICKENPOX VACCINE; COTRIMOXAZOLE; CYTOKINE; FLUCONAZOLE; FLUDARABINE; IMMUNOGLOBULIN; LYMPHOCYTE ANTIGEN RECEPTOR; MELPHALAN; STEROID;

ALLELE; ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; B LYMPHOCYTE; CASE REPORT; CELL COMPARTMENTALIZATION; CHICKENPOX; CHILD; CHROMOSOME 16P11.2 DELETION; CHROMOSOME DELETION; CORONIN 1A GENE; CYTOSKELETON; DISEASE SEVERITY; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; GENETIC VARIABILITY; GENOME; GRAFT VERSUS HOST REACTION; HUMAN; NATURAL KILLER CELL; PNEUMOCYSTOSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; RECURRENT INFECTION; SEVERE COMBINED IMMUNODEFICIENCY; SIGNAL TRANSDUCTION; T LYMPHOCYTE; THRUSH; THYMUS;

ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 16; DNA; FEMALE; HUMANS; INFANT; MICROFILAMENT PROTEINS; MUTATION; SEQUENCE ANALYSIS, DNA; SEVERE COMBINED IMMUNODEFICIENCY; T-LYMPHOCYTES; THYMUS GLAND;

EID: 63249106283     PISSN: 15216616     EISSN: 15217035     Source Type: Journal    
DOI: 10.1016/j.clim.2008.11.002     Document Type: Article

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