Mutation of the BTK gene and clinical feature of X-linked agammaglobulinemia in mainland China

Journal of Clinical Immunology

Volumn 29, Issue 3, 2009, Pages 352-356

  Wang, Ying ^a   Kanegane, Hirokazu ^b   Wang, Xiaochuan ^a   Han, Xiaohua ^c   Zhang, Qian ^a   Zhao, Shunying ^d   Yu, Yeheng ^a   Wang, Jingyi ^a   Miyawaki, Toshio ^b  

^a CHILDREN S HOSPITAL OF FUDAN UNIVERSITY   (China)

^b UNIVERSITY OF TOYAMA   (Japan)

^c CHINA MEDICAL UNIVERSITY   (China)

^d CAPITAL MEDICAL UNIVERSITY   (China)

Author keywords

Bruton's tyrosine kinase; Humoral immunodeficiency; Mutation; X linked agammaglobulinemia

Indexed keywords

AMINO ACID; BRUTON TYROSINE KINASE; IMMUNOGLOBULIN; NUCLEOTIDE; PLECKSTRIN;

ADOLESCENT; ADULT; ARTICLE; BTK GENE; CHILD; CHINA; CHINESE; CLINICAL ARTICLE; CLINICAL FEATURE; FAMILY; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENOTYPE; HUMAN; IMMUNOGLOBULIN BLOOD LEVEL; INTRON; LIVER CANCER; MALE; MISSENSE MUTATION; MOLECULAR GENETICS; MOTHER; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DOMAIN; SEQUENCE HOMOLOGY; X LINKED AGAMMAGLOBULINEMIA;

ADOLESCENT; ADULT; AGAMMAGLOBULINEMIA; BACTERIAL INFECTIONS; CHILD; CHILD, PRESCHOOL; CHINA; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUTATION; OPPORTUNISTIC INFECTIONS; PNEUMONIA; PROTEIN-TYROSINE KINASES; SINUSITIS; X-LINKED COMBINED IMMUNODEFICIENCY DISEASES;

EID: 67349160500     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-008-9262-8     Document Type: Article

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