Warren, Mikako <br/><br/>
Association of a de novo nonsense mutation of the TRIM8 gene with childhood-onset focal segmental glomerulosclerosis.  [electronic resource] 

 -  Pediatric nephrology (Berlin, Germany)  06 2020 
 - 1129-1132 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/s00467-020-04525-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carrier Proteins<br/>Child<br/>Codon, Nonsense--genetics<br/>Drug Resistant Epilepsy--complications<br/>Glomerulosclerosis, Focal Segmental--diagnosis<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Male<br/>Nerve Tissue Proteins<br/>Podocytes--metabolism<br/>Suppressor of Cytokine Signaling 1 Protein