Registries of immunodeficiency patients and mutations

Human Mutation

Volumn 10, Issue 4, 1997, Pages 261-267

  Lappalainen, Ilkka ^a   Ollila, Juha ^a   Smith, C I Edvard ^b,c   Vihinen, Mauno ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

^b KAROLINSKA INSTITUTE   (Sweden)

^c KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

CGD; Immunodeficiencies; Mutation registries CpG dinucleotides; SCID; WAS; XHIM; XLA; XLT

Indexed keywords

AMINO ACID; CD40 ANTIGEN; CYTOKINE; DINUCLEOTIDE; ENZYME; IMMUNOGLOBULIN M; MAJOR HISTOCOMPATIBILITY ANTIGEN; PROTEIN; PROTEIN TYROSINE KINASE; RECEPTOR;

CHRONIC GRANULOMATOUS DISEASE; DATA BASE; GENE; HUMAN; HYPERIMMUNOGLOBULINEMIA; IMMUNE DEFICIENCY; INTERNET; MAJOR CLINICAL STUDY; MUTATION; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; REGISTER; REVIEW; THROMBOCYTOPENIA; WISKOTT ALDRICH SYNDROME; X CHROMOSOME;

ALLERGY AND IMMUNOLOGY; DATABASES; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; MUTATION; REGISTRIES; TERMINOLOGY;

EID: 0030924024     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1997)10:4<261::AID-HUMU1>3.0.CO;2-K     Document Type: Review

References (5)

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3. Anderson DC, Schmalstieg FC, Arnaout MA, Kohl S, Tosi MF, Dana N, Buffone GJ, Hughes BJ, Brinkley BR, Dickey WD, et al. (1984) Abnormalities of polymorphonuclear leukocyte function associated with a heritable deficiency of high molecular weight surface glycoproteins (GP138): common relationship to diminished cell adherence. J Clin Invest 74:536-551.
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