1. Gowda, Vykuntaraju K, Srinivasan, Varunvenkat M, Vegda, Hemadri, Bhat, Maya. 2020. Fucosidosis with Pathogenic Variant in FUCA1 Gene. In Indian journal of pediatrics, 87, 867-868. doi:10.1007/s12098-020-03246-7. https://pubmed.ncbi.nlm.nih.gov/32125660/
2. Wali, Gautam, Wali, G M, Sue, Carolyn M, Kumar, Kishore R. 2019. A Novel Homozygous Mutation in the FUCA1 Gene Highlighting Fucosidosis as a Cause of Dystonia: Case Report and Literature Review. In Neuropediatrics, 50, 248-252. doi:10.1055/s-0039-1684052. https://pubmed.ncbi.nlm.nih.gov/31064022/
3. Ezawa, Issei, Sawai, Yuichiro, Kawase, Tatsuya, Nakagama, Hitoshi, Ohki, Rieko. 2016. Novel p53 target gene FUCA1 encodes a fucosidase and regulates growth and survival of cancer cells. In Cancer science, 107, 734-45. doi:10.1111/cas.12933. https://pubmed.ncbi.nlm.nih.gov/26998741/
4. do Rosario, Michelle C, Purushothama, Greeshma, Narayanan, Dhanya Lakshmi, Girisha, Katta Mohan, Shukla, Anju. 2023. Extended analysis of exome sequencing data reveals a novel homozygous deletion of exons 3 and 4 in FUCA1 gene causing fucosidosis in an Indian family. In Clinical dysmorphology, 32, 112-115. doi:10.1097/MCD.0000000000000452. https://pubmed.ncbi.nlm.nih.gov/36876340/
5. Baudot, Alice D, Wang, Victoria M-Y, Leach, Josh D, Zanivan, Sara, Ryan, Kevin M. 2022. Glycan degradation promotes macroautophagy. In Proceedings of the National Academy of Sciences of the United States of America, 119, e2111506119. doi:10.1073/pnas.2111506119. https://pubmed.ncbi.nlm.nih.gov/35737835/
6. Saleh-Gohari, Nasrollah, Saeidi, Kolsoum, Zeighaminejad, Roya. 2018. A novel homozygous frameshift mutation in the FUCA1 gene causes both severe and mild fucosidosis. In Journal of clinical pathology, 71, 821-824. doi:10.1136/jclinpath-2018-205074. https://pubmed.ncbi.nlm.nih.gov/29588375/