WHOLE EXOME SEQUENCING OF TWO RARE FAMILIAL COHORTS IDENTIFIES PUTATIVE GENETIC VARIANTS IN CHILDHOOD SJOGREN'S DISEASE Meeting Abstract

International Collaboration

cited authors

  • Winn, N.; Kim, S.; Mun, S.; Khan, Z.; Thatayatikom, A.; Han, K.; Cha, S.

authors

Publication Date

  • December 1, 2022

webpage

published in

category

start page

  • 26

end page

  • 26

volume

  • 40

issue

  • 12