1. Wang, Sai, Yue, Yuanyi, Wang, Xueqing, Tan, Yue, Zhang, Qiang. 2024. SCARF2 is a target for chronic obstructive pulmonary disease: Evidence from multi-omics research and cohort validation. In Aging cell, 23, e14266. doi:10.1111/acel.14266. https://pubmed.ncbi.nlm.nih.gov/38958042/
2. Vo, Thuy-Trang T, Kong, Gyeyeong, Kim, Chaeyeong, Kim, Seon-Hwan, Park, Jongsun. 2023. Exploring scavenger receptor class F member 2 and the importance of scavenger receptor family in prediagnostic diseases. In Toxicological research, 39, 341-353. doi:10.1007/s43188-023-00176-2. https://pubmed.ncbi.nlm.nih.gov/37398563/
3. Anastasio, Natascia, Ben-Omran, Tawfeg, Teebi, Ahmad, Majewski, Jacek, Jerome-Majewska, Loydie A. . Mutations in SCARF2 are responsible for Van Den Ende-Gupta syndrome. In American journal of human genetics, 87, 553-9. doi:10.1016/j.ajhg.2010.09.005. https://pubmed.ncbi.nlm.nih.gov/20887961/
4. Hildebrandt, Clara C, Patel, Nisha, Graham, John M, Alkuraya, Fowzan S, Lin, Angela E. 2021. Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome. In American journal of medical genetics. Part A, 185, 2136-2149. doi:10.1002/ajmg.a.62194. https://pubmed.ncbi.nlm.nih.gov/33783941/
智鼠故事 
