1. Zhou, Cheng, Wang, Pei, Yang, Dingquan, Wang, Rongrong, Zhang, Jianzhong. 2022. Autosomal recessive monilethrix: Novel variants of the DSG4 gene in three Chinese families. In Molecular genetics & genomic medicine, 10, e1889. doi:10.1002/mgg3.1889. https://pubmed.ncbi.nlm.nih.gov/35146972/
2. Moreno-Sosa, Tamara, Sánchez, María Belén, Pietrobon, Elisa Olivia, Valdez, Susana Ruth, Mackern-Oberti, Juan Pablo. 2021. Desmoglein-4 Deficiency Exacerbates Psoriasiform Dermatitis in Rats While Psoriasis Patients Displayed a Decreased Gene Expression of DSG4. In Frontiers in immunology, 12, 625617. doi:10.3389/fimmu.2021.625617. https://pubmed.ncbi.nlm.nih.gov/33995349/
3. Kiener, Sarah, Rostaher, Ana, Rüfenacht, Silvia, Welle, Monika, Leeb, Tosso. 2021. Independent DSG4 frameshift variants in cats with hair shaft dystrophy. In Molecular genetics and genomics : MGG, 297, 147-154. doi:10.1007/s00438-021-01842-6. https://pubmed.ncbi.nlm.nih.gov/34878611/
4. Ullah, A, Raza, S I, Ali, R H, Satti, R, Ahmad, W. 2014. A novel deletion mutation in the DSG4 gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families. In Clinical and experimental dermatology, 40, 78-84. doi:10.1111/ced.12457. https://pubmed.ncbi.nlm.nih.gov/25251037/
5. Wang, Jia-Man, Xiao, Yu-Juan, Liang, Yan-Hua. 2015. Novel D323G mutation of DSG4 gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix. In International journal of dermatology, 54, 1163-8. doi:10.1111/ijd.12889. https://pubmed.ncbi.nlm.nih.gov/26173648/
6. E, G X, Zhao, Y J, Ma, Y H, Hu, W, Huang, Y F. 2016. Desmoglein 4 diversity and correlation analysis with coat color in goat. In Genetics and molecular research : GMR, 15, 15017814. doi:10.4238/gmr.15017814. https://pubmed.ncbi.nlm.nih.gov/26985930/
7. Rafiq, Muhammad Arshad, Ansar, Muhammad, Mahmood, Saqib, Leal, Suzanne M, Ahmad, Wasim. . A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis. In The Journal of investigative dermatology, 123, 247-8. doi:. https://pubmed.ncbi.nlm.nih.gov/15191570/
8. Kato, Madoka, Shimizu, Akira, Yokoyama, Yoko, Tokunaga, Fuminori, Ishikawa, Osamu. 2015. An autosomal recessive mutation of DSG4 causes monilethrix through the ER stress response. In The Journal of investigative dermatology, 135, 1253-1260. doi:10.1038/jid.2015.12. https://pubmed.ncbi.nlm.nih.gov/25615553/
智鼠故事 
