Lv, Fang <br/><br/>
Recurrent and novel mutations in the NTRK1 gene lead to rare congenital insensitivity to pain with anhidrosis in two Chinese patients.  [electronic resource] 

 -  Clinica chimica acta; international journal of clinical chemistry  May 2017 
 - 39-45 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1873-3492 
<br/><br/><label>Standard No.: </label>10.1016/j.cca.2017.02.007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Asian People--genetics<br/>Base Sequence<br/>Child<br/>Female<br/>Hereditary Sensory and Autonomic Neuropathies--enzymology<br/>Humans<br/>Male<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Receptor, trkA--chemistry<br/>Young Adult