1. Wang, Yujuan, Lan, Xinqiang. . [Analysis of SUOX gene variants and clinical features in a child with Isolated sulfite oxidase deficiency]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 40, 177-180. doi:10.3760/cma.j.cn511380-20210702-00563. https://pubmed.ncbi.nlm.nih.gov/36709936/
2. 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/
3. 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/
4. 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/
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/
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