Wang, Yanyan <br/><br/>
Clinical and genetic features in autosomal recessive and X-linked Alport syndrome.  [electronic resource] 

 -  Pediatric nephrology (Berlin, Germany)  Mar 2014 
 - 391-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-198X 
<br/><br/><label>Standard No.: </label>10.1007/s00467-013-2643-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>DNA Mutational Analysis<br/>Female<br/>Genes, X-Linked<br/>Genetic Predisposition to Disease<br/>Genetic Testing--methods<br/>Hearing Loss--genetics<br/>Heredity<br/>Humans<br/>Kidney Failure, Chronic--genetics<br/>Male<br/>Middle Aged<br/>Mutation<br/>Nephritis, Hereditary--complications<br/>Pedigree<br/>Phenotype<br/>Predictive Value of Tests<br/>Prognosis<br/>Retinal Diseases--genetics<br/>Risk Factors<br/>Sex Factors<br/>Time Factors<br/>Young Adult