Lo, Fu-Sung <br/><br/>
Two novel PHEX mutations in Taiwanese patients with X-linked hypophosphatemic rickets.  [electronic resource] 

 -  Nephron. Physiology  2006 
 - p157-63 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1660-2137 
<br/><br/><label>Standard No.: </label>10.1159/000092916  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Female<br/>Humans<br/>Hypophosphatemia, Familial--diagnosis<br/>Infant<br/>Male<br/>Membrane Glycoproteins--genetics<br/>Metalloendopeptidases--genetics<br/>Mutation<br/>PHEX Phosphate Regulating Neutral Endopeptidase<br/>Pedigree<br/>Radiography<br/>Taiwan