1. Li, Jia-Tong, Chen, Ze-Xu, Chen, Xiang-Jun, Jiang, Yong-Xiang. 2022. Mutation analysis of SUOX in isolated sulfite oxidase deficiency with ectopia lentis as the presenting feature: insights into genotype-phenotype correlation. In Orphanet journal of rare diseases, 17, 392. doi:10.1186/s13023-022-02544-x. https://pubmed.ncbi.nlm.nih.gov/36303223/
2. Zhang, Rui, Hao, Yajing, Xu, Ying, Wang, Huilin, Banerjee, Santasree. 2022. Whole exome sequencing identified a homozygous novel mutation in SUOX gene causes extremely rare autosomal recessive isolated sulfite oxidase deficiency. In Clinica chimica acta; international journal of clinical chemistry, 532, 115-122. doi:10.1016/j.cca.2022.06.005. https://pubmed.ncbi.nlm.nih.gov/35679912/
3. Claerhout, Helena, Witters, Peter, Régal, Luc, Breckpot, Jeroen, Vermeersch, Pieter. 2017. Isolated sulfite oxidase deficiency. In Journal of inherited metabolic disease, 41, 101-108. doi:10.1007/s10545-017-0089-4. https://pubmed.ncbi.nlm.nih.gov/28980090/
4. Nakamura, Ken, Akiba, Jun, Ogasawara, Sachiko, Kusukawa, Jingo, Yano, Hirohisa. 2017. SUOX is negatively associated with multistep carcinogenesis and proliferation in oral squamous cell carcinoma. In Medical molecular morphology, 51, 102-110. doi:10.1007/s00795-017-0177-4. https://pubmed.ncbi.nlm.nih.gov/29280012/
5. Zhao, Jiangang, An, Yao, Jiang, Haoxiang, Che, Fengyu, Yang, Ying. 2021. Novel Compound Heterozygous Pathogenic Variants in SUOX Cause Isolated Sulfite Oxidase Deficiency in a Chinese Han Family. In Frontiers in genetics, 12, 607085. doi:10.3389/fgene.2021.607085. https://pubmed.ncbi.nlm.nih.gov/34025712/
6. Du, Peng, Hassan, Reem N, Luo, Hualei, Yan, Jin, Jiang, Weiying. 2021. Identification of a novel SUOX pathogenic variants as the cause of isolated sulfite oxidase deficiency in a Chinese pedigree. In Molecular genetics & genomic medicine, 9, e1590. doi:10.1002/mgg3.1590. https://pubmed.ncbi.nlm.nih.gov/33405344/
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