Classification of primary immunodeficiency disorders: One-fits-all does not help anymore

Clinical Immunology

Volumn 144, Issue 1, 2012, Pages 24-25

  Al Herz, Waleed ^a   Notarangelo, Luigi D ^b  

^a KUWAIT UNIVERSITY   (Kuwait)

^b BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

Classification; Genetics; Phenotype; Primary immunodeficiency

Indexed keywords

INTERLEUKIN 17 RECEPTOR; INTERLEUKIN 17F; STAT1 PROTEIN;

DISEASE CLASSIFICATION; DNA SEQUENCE; GAIN OF FUNCTION MUTATION; GENE IDENTIFICATION; GENETIC COUNSELING; GENETIC LINKAGE; GENETIC VARIABILITY; HUMAN; IMMUNE DEFICIENCY; LETTER; LOSS OF FUNCTION MUTATION; MUCOCUTANEOUS CANDIDIASIS; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; WHOLE EXOME SEQUENCING; WHOLE GENOME SEQUENCING;

HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; MUTATION; PHENOTYPE;

EID: 84861555765     PISSN: 15216616     EISSN: 15217035     Source Type: Journal    
DOI: 10.1016/j.clim.2012.05.003     Document Type: Letter

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