Barone, R <br/><br/>
Congenital insensitivity to pain with Anhidrosis (NTRK1 mutation) and early onset renal disease: clinical report on three sibs with a 25-year follow-up in one of them.  [electronic resource] 

 -  Neuropediatrics  Aug 2005 
 - 270-3 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0174-304X 
<br/><br/><label>Standard No.: </label>10.1055/s-2005-872808  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>B-Lymphocytes--metabolism<br/>CD5 Antigens--metabolism<br/>Child<br/>DNA Mutational Analysis--methods<br/>Female<br/>Humans<br/>Hypohidrosis--etiology<br/>Immunoglobulin G--urine<br/>Longitudinal Studies<br/>Male<br/>Mutation<br/>Pain Insensitivity, Congenital--complications<br/>Receptor, trkA--genetics<br/>Siblings