A novel loss-of-function mutation in LACC1 underlies hereditary juvenile arthritis with extended intra-familial phenotypic heterogeneity

Back to Abstracts

A novel loss-of-function mutation in LACC1 underlies hereditary juvenile arthritis with extended intra-familial phenotypic heterogeneity

  • Yonatan Butbul Aviel, MD, Ayala Ofir, PhD,Ofer Ben-Izhak, MD, Euvgeni Vlodavsky, MD, Netanel Karbian, PhD, Riva Brik, MD, Dror Mevorach, MD, Daniella Magen, MD
Previous E-Poster Download E-Poster Next E-Poster