Yu-Ri Lee

Years Active: 2020-2021
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Yu-Ri Lee, Se Hee Kim, Afif Ben-Mahmoud, Oc-Hee Kim, Tae-Ik Choi, Kang-Han Lee, Bonsu Ku, Juneyong Eum, Yun Kee, Sangkyu Lee, Jihoon Cha, DongJu Won, Seung-Tae Lee, Jong Rak Choi, Joon Soo Lee, Heung Dong Kim, Hyung-Goo Kim, Joshua L Bonkowsky, Hoon-Chul Kang, Cheol-Hee Kim
Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish. Human molecular genetics 30 (5) (2021)
Yu-Ri Lee, Kamal Khan, Kim Armfield-Uhas, Sujata Srikanth, Nicola A Thompson, Mercedes Calvo Pardo, Lu Yu, Joy W Norris, Yunhui Peng, Karen W Gripp, Kirk A Aleck, Chumei Li, Ed Spence, Tae-Ik Choi, Soo Jeong Kwon, Hee-Moon Park, Daseuli Yu, Seokhwi Kim, Marie R Mooney, Shahid M Baig, Ingrid M Wentzensen, Aida Telegrafi, Kirsty McWalter, Trevor A Moreland, Chelsea Roadhouse, Keri Ramsey, Michael J Lyons, Cindy Skinner, Emil Alexov, Nicholas Katsanis, Roger E Stevenson, Jyoti Sharma Choudhary, David J Adams, Cheol-Hee Kim, Erica E Davis, Charles E Schwartz
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy. Nature communications 11 (1) (2020)

Yu-Ri Lee.css-eqlu8i{font-size:small;padding-left:4px;}