Li, Yanhan <br/><br/>
A novel mutation associated with Type III Bartter syndrome: A report of five cases.  [electronic resource] 

 -  Molecular medicine reports  Jul 2019 
 - 65-72 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1791-3004 
<br/><br/><label>Standard No.: </label>10.3892/mmr.2019.10255  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Amniocentesis--methods<br/>Bartter Syndrome--diagnosis<br/>Child<br/>Child, Preschool<br/>Chloride Channels--genetics<br/>Female<br/>Humans<br/>Infant<br/>Insulin-Like Growth Factor I--genetics<br/>Male<br/>Mutation--genetics<br/>Phenotype<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Sequence Deletion<br/>Young Adult