Lv, Fang <br/><br/>
A novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family.  [electronic resource] 

 -  Clinica chimica acta; international journal of clinical chemistry  Jun 2016 
 - 69-74 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.2016.04.004  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>China<br/>Claudins--genetics<br/>Ethnicity<br/>Female<br/>Humans<br/>Hypercalciuria--complications<br/>Magnesium--blood<br/>Male<br/>Mutation<br/>Nephrocalcinosis--complications<br/>Pedigree