Beauregard-Lacroix, Eliane <br/><br/>
A variant of neonatal progeroid syndrome, or Wiedemann-Rautenstrauch syndrome, is associated with a nonsense variant in POLR3GL.  [electronic resource] 

 -  European journal of human genetics : EJHG  04 2020 
 - 461-468 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/s41431-019-0539-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Codon, Nonsense<br/>Female<br/>Fetal Growth Retardation--genetics<br/>Humans<br/>Phenotype<br/>Progeria--genetics<br/>Protein Domains<br/>RNA Polymerase III--chemistry