Eng, C <br/><br/>
A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC.  [electronic resource] 

 -  Oncogene  Feb 1995 
 - 509-13 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0950-9232 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Carcinoma, Medullary--genetics<br/>Codon--genetics<br/>Drosophila Proteins<br/>Female<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Multiple Endocrine Neoplasia--genetics<br/>Pedigree<br/>Point Mutation<br/>Proto-Oncogene Mas<br/>Proto-Oncogene Proteins--genetics<br/>Proto-Oncogene Proteins c-ret<br/>Proto-Oncogenes--genetics<br/>Receptor Protein-Tyrosine Kinases--genetics<br/>Thyroid Neoplasms--genetics