Saffran, D C <br/><br/>
Brief report: a point mutation in the SH2 domain of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia.  [electronic resource] 

 -  The New England journal of medicine  May 1994 
 - 1488-91 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0028-4793 
<br/><br/><label>Standard No.: </label>10.1056/NEJM199405263302104  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Agammaglobulinaemia Tyrosine Kinase<br/>Agammaglobulinemia--enzymology<br/>Amino Acid Sequence<br/>Base Sequence<br/>Cell Line, Transformed<br/>Enzyme Stability--genetics<br/>Female<br/>Genetic Linkage<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Protein-Tyrosine Kinases--analysis<br/>RNA, Messenger--analysis<br/>X Chromosome