Abstract
A first report of an XLA patient with a polymorphism in Btk SH3 domain has been identified after sequencing of the entire gene. SH3 domain variants might not be detected due to well characterized mutations outside the domain.
Publication types
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Letter
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Research Support, Non-U.S. Gov't
MeSH terms
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Agammaglobulinaemia Tyrosine Kinase
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Agammaglobulinemia / enzymology*
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Agammaglobulinemia / genetics*
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Child, Preschool
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Female
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Genetic Diseases, X-Linked / enzymology*
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Humans
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Infant
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Male
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Mutation / genetics*
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Pedigree
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Protein Structure, Secondary
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Protein-Tyrosine Kinases / chemistry*
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Protein-Tyrosine Kinases / genetics*
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src Homology Domains*
Substances
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Protein-Tyrosine Kinases
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Agammaglobulinaemia Tyrosine Kinase
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BTK protein, human