A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome

Journal of Clinical Investigation

Volumn 97, Issue 1, 1996, Pages 196-201

  Lin, Qiong ^a   Rohrer, Jürg ^a   Allen, R Cutler ^b   Larché, Mark ^a   Greene, Jeffrey M ^c   Shigeoka, Ann O ^d   Gatti, Richard A ^e   Derauf, D Christian ^f   Belmont, John W ^b   Conley, Mary Ellen ^a,g  

^a ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^d UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

^f KAPIOLANI MEDICAL CENTER FOR WOMEN AND CHILDREN   (United States)

^g UNIVERSITY OF TENNESSEE COLLEGE OF MEDICINE   (United States)

Author keywords

agammaglobulinemia; DNA, mutational analysis; gene deletion; genetic counseling; hypergammaglobulinemia, genetics

Indexed keywords

CD40 ANTIGEN; IMMUNOGLOBULIN M;

ARTICLE; CLINICAL ARTICLE; GENE DELETION; GENE MUTATION; HETEROZYGOTE DETECTION; HUMAN; HUMAN CELL; HYPERGAMMAGLOBULINEMIA; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; T LYMPHOCYTE ACTIVATION; X CHROMOSOME LINKED DISORDER;

EID: 13344280345     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI118389     Document Type: Article

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