Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1996-3-27
pubmed:abstractText
Bruton's tyrosine kinase (Btk) has been identified as the protein responsible for the primary immunodeficiency X-linked agammaglobulinemia (XLA). We and others have cloned the gene for Btk and recently reported the genomic organization. Nineteen exons were positioned within the 37 kb gene. With the sequence data derived from our genomic map, we have designed a PCR based assay to directly identify mutations of the Btk gene in germline DNA of patients with XLA. In this report, the assay was used to analyze a family with a sporadic case of XLA to determine if other female relatives carry the disease. A four base-pair deletion was found in the DNA of the affected boy and was further traced through three generations. With the direct identification of the mutations responsible for XLA, we can now diagnose conclusively the disease and identify the immunologically normal female carriers. This same technique can easily be applied to prenatal diagnosis in families where the mutation can be identified.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0148-7299
pubmed:author
pubmed:issnType
Print
pubmed:day
6
pubmed:volume
59
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
188-92
pubmed:dateRevised
2011-11-2
pubmed:meshHeading
pubmed-meshheading:8588584-Agammaglobulinemia, pubmed-meshheading:8588584-Amino Acid Sequence, pubmed-meshheading:8588584-Base Sequence, pubmed-meshheading:8588584-Child, Preschool, pubmed-meshheading:8588584-DNA, pubmed-meshheading:8588584-DNA Mutational Analysis, pubmed-meshheading:8588584-Female, pubmed-meshheading:8588584-Genetic Linkage, pubmed-meshheading:8588584-Heterozygote Detection, pubmed-meshheading:8588584-Humans, pubmed-meshheading:8588584-Male, pubmed-meshheading:8588584-Molecular Sequence Data, pubmed-meshheading:8588584-Pedigree, pubmed-meshheading:8588584-Polymerase Chain Reaction, pubmed-meshheading:8588584-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:8588584-Protein-Tyrosine Kinases, pubmed-meshheading:8588584-Sequence Deletion, pubmed-meshheading:8588584-X Chromosome
pubmed:year
1995
pubmed:articleTitle
Mutation analysis of the gene encoding Bruton's tyrosine kinase in a family with a sporadic case of X-linked agammaglobulinemia reveals three female carriers.
pubmed:affiliation
Department of Immunology/Microbiology, Rush Medical School, Chicago, IL 60612, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Case Reports, Research Support, Non-U.S. Gov't