1. Yang, P, Zeng, C Z, Tao, X W, Long, Y, Zeng, L K. . [Zellweger syndrome caused by PEX6 gene variation in 2 cases and literature review]. In Zhonghua er ke za zhi = Chinese journal of pediatrics, 62, 43-48. doi:10.3760/cma.j.cn112140-20230914-00191. https://pubmed.ncbi.nlm.nih.gov/38154976/
2. Benson, Matthew D, Papp, Kimberly M, Casey, Geoffrey A, Doucette, Lance P, MacDonald, Ian M. 2021. PEX6 Mutations in Peroxisomal Biogenesis Disorders: An Usher Syndrome Mimic. In Ophthalmology science, 1, 100028. doi:10.1016/j.xops.2021.100028. https://pubmed.ncbi.nlm.nih.gov/36249295/
3. Slaton, Daniel, Chang, Ashley, Ahluwalia, Tamanna, Javed, Britani, Greer, Rocky. 2023. Zellweger's Syndrome With PEX6 Gene Mutation in Mixteco Neonates Due to Possible Founder Effect. In Cureus, 15, e45162. doi:10.7759/cureus.45162. https://pubmed.ncbi.nlm.nih.gov/37842507/
4. Yang, Pin, Zhang, Weihong, Zeng, Lingkong, Ding, Kaiwei, Wang, Zuo. 2024. A novel splice variant in intron 10 of PEX6 is associated with Zellweger Syndrome in a Chinese neonate. In Gene, 928, 148767. doi:10.1016/j.gene.2024.148767. https://pubmed.ncbi.nlm.nih.gov/39013483/
5. Smith, Claire E L, Poulter, James A, Levin, Alex V, Mighell, Alan J, Inglehearn, Chris F. 2016. Spectrum of PEX1 and PEX6 variants in Heimler syndrome. In European journal of human genetics : EJHG, 24, 1565-1571. doi:10.1038/ejhg.2016.62. https://pubmed.ncbi.nlm.nih.gov/27302843/
6. Ebberink, Merel S, Kofster, Janet, Wanders, Ronald J A, Waterham, Hans R. . Spectrum of PEX6 mutations in Zellweger syndrome spectrum patients. In Human mutation, 31, E1058-70. doi:10.1002/humu.21153. https://pubmed.ncbi.nlm.nih.gov/19877282/
7. Slanina, Ana-Maria, Coman, Adorata-Elena, Anton-Păduraru, Dana-Teodora, Manole, Mihaela, Cosmescu, Adriana. 2023. PEX6 Mutation in a Child with Infantile Refsum Disease-A Case Report and Literature Review. In Children (Basel, Switzerland), 10, . doi:10.3390/children10030530. https://pubmed.ncbi.nlm.nih.gov/36980088/
8. Galarreta, Carolina I, Wong, Karen, Carmichael, Jason, Verscaj, Courtney P, Cusmano-Ozog, Kristina P. 2023. A homozygous Gly470Ala variant in PEX6 causes severe Zellweger spectrum disorder. In American journal of medical genetics. Part A, 191, 2057-2063. doi:10.1002/ajmg.a.63234. https://pubmed.ncbi.nlm.nih.gov/37144748/
智鼠故事 
