Novel Compound Heterozygote Variations in FADD Identified to Cause FAS-Associated Protein with Death Domain Deficiency

por Kohn, Lisa A., Long, Joseph D., Trope, Edward C., Kuo, Caroline Y.
Publicado 2020

Ocular findings associated with FADD deficiency resemble familial exudative vitreoretinopathy

por Meer, Elana, Solanes, Federica, Kohn, Lisa, Kuo, Caroline Y., Wong, Derek A., Pineles, Stacy, Tsui, Irena
Publicado 2022

A comparison of DNA repair pathways to achieve a site-specific gene modification of the Bruton's tyrosine kinase gene

por Gray, David H., Santos, Jasmine, Keir, Alexandra Grace, Villegas, Isaac, Maddock, Simon, Trope, Edward C., Long, Joseph D., Kuo, Caroline Y.
Publicado 2021