Yiş, Uluç <br/><br/>
A novel NTRK1 mutation in a patient with congenital insensitivity to pain with anhidrosis.  [electronic resource] 

 -  Acta neurologica Belgica  Sep 2015 
 - 509-11 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2240-2993 
<br/><br/><label>Standard No.: </label>10.1007/s13760-014-0405-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Child<br/>Hereditary Sensory and Autonomic Neuropathies--genetics<br/>Humans<br/>Male<br/>Mutation<br/>Pedigree<br/>Receptor, trkA--genetics