Unique combination and in silico modeling of biallelic POLR3A variants as a cause of WiedemannâRautenstrauch syndrome
Temel, Sehime Gulsun, Ergoren, Mahmut Cerkez, Manara, Elena, Paolacci, Stefano, Tuncel, Gulten, Gul, Seref, Bertelli, MatteoJournal:
European Journal of Human Genetics
DOI:
10.1038/s41431-020-0673-1
Date:
June, 2020
File:
PDF, 1.76 MB
2020