For: | Li ZR, Zhou YL, Jin Q, Xie YY, Meng HM. CYP27A1 mutation in a case of cerebrotendinous xanthomatosis: A case report. World J Clin Cases 2022; 10(18): 6168-6174 [PMID: 35949830 DOI: 10.12998/wjcc.v10.i18.6168] |
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URL: | https://www.wjgnet.com/2307-8960/full/v10/i18/6168.htm |
Number | Citing Articles |
1 |
Petar Brlek, Luka Bulić, David Glavaš Weinberger, Jelena Bošnjak, Tomislav Pavlović, Svetlana Tomić, Zdravka Krivdić Dupan, Igor Borić, Dragan Primorac. Successful Treatment of a Rare Cholesterol Homeostasis Disorder Due to CYP27A1 Gene Mutation with Chenodeoxycholic Acid Therapy. Biomedicines 2023; 11(5): 1430 doi: 10.3390/biomedicines11051430
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2 |
Zahra Beyzaei, Hossein Moravej, Mohammad Hadi Imanieh, Sorour Inaloo, Bita Geramizadeh. Identification of two Iranian siblings with cerebrotendinous xanthomatosis: a case report. Egyptian Journal of Medical Human Genetics 2023; 24(1) doi: 10.1186/s43042-023-00413-1
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3 |
You Guoliang, Wang Zhaoxia, Zhang Lin, Chen Xuan, Zhang Xiaodong, Xing Xiaolian, Su Yangli, Zhang Tianli, Zhu Yanping, Wang Jiangping, Liu Qing. Clinical and genetic analysis of a family with cerebrotendinous xanthomatosis. Frontiers in Neurology 2025; 16 doi: 10.3389/fneur.2025.1566740
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