Coding-region alterations in BTK do not universally cause X-linked agammaglobulinemia

Journal of Allergy and Clinical Immunology

Volumn 132, Issue 5, 2013, Pages 1246-1248

  Abbott, Jordan K ^a   Ochs, Hans D ^b,c   Gelfand, Erwin W ^a  

^a DEPARTMENT OF MEDICINE   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^c SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

B LYMPHOCYTE; BTK GENE; GENE; GENE MUTATION; GENETIC CODE; GENETIC VARIABILITY; HUMAN; HUMAN CELL; HUMORAL IMMUNE DEFICIENCY; LABORATORY TEST; LETTER; MISSENSE MUTATION; PATHOGENICITY; PRIORITY JOURNAL; X LINKED AGAMMAGLOBULINEMIA;

EID: 84887021474     PISSN: 00916749     EISSN: 10976825     Source Type: Journal    
DOI: 10.1016/j.jaci.2013.07.019     Document Type: Article

References (10)

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