1. Richardson, Brian C, Smith, Richard D, Ungar, Daniel, Lupashin, Vladimir V, Hughson, Frederick M. 2009. Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene. In Proceedings of the National Academy of Sciences of the United States of America, 106, 13329-34. doi:10.1073/pnas.0901966106. https://pubmed.ncbi.nlm.nih.gov/19651599/
2. Xiao, Binghe, Zhang, Shaohua, Ainiwaer, Maierdanjiang, Sun, Yang, Ji, Yinghong. 2025. Deep learning-based assessment of missense variants in the COG4 gene presented with bilateral congenital cataract. In BMJ open ophthalmology, 10, . doi:10.1136/bmjophth-2024-001906. https://pubmed.ncbi.nlm.nih.gov/39809522/
3. Sumya, Farhana Taher, Pokrovskaya, Irina D, Lupashin, Vladimir. 2021. Development and Initial Characterization of Cellular Models for COG Complex-Related CDG-II Diseases. In Frontiers in genetics, 12, 733048. doi:10.3389/fgene.2021.733048. https://pubmed.ncbi.nlm.nih.gov/34603392/
4. Zafra, Isabella, Nebenfuehr, Benjamin, Golden, Andy. 2021. Saul-Wilson Syndrome Missense Allele Does Not Show Obvious Golgi Defects in a C. elegans Model. In microPublication biology, 2021, . doi:10.17912/micropub.biology.000373. https://pubmed.ncbi.nlm.nih.gov/33688625/
智鼠故事 
