Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype

Por Kamath-Loeb, Ashwini S., Zavala-van Rankin, Diego G., Flores-Morales, Jeny, Emond, Mary J., Sidorova, Julia M., Carnevale, Alessandra, Cárdenas-Cortés, Maria del Carmen, Norwood, Thomas H., Monnat, Raymond J., Loeb, Lawrence A., Mercado-Celis, Gabriela E.
Publicado no Sci Rep (2017)