| For: | Ye S, Gong L, Shui QX, Zhou LF. Wilson disease: Identification of two novel mutations and clinical correlation in Eastern Chinese patients. World J Gastroenterol 2007; 13(38): 5147-5150 [PMID: 17876883 DOI: 10.3748/wjg.v13.i38.5147] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v13/i38/5147.htm |
| Number | Citing Articles |
| 1 |
Juan Geng, Jian Wang, Ru-En Yao, Xiao-Qing Liu, Qi-Hua Fu. Identification of one novel and nine recurrent mutations of the ATP7B gene in 11 children with Wilson disease. World Journal of Pediatrics 2013; 9(2) doi: 10.1007/s12519-012-0388-7
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| 2 |
Mingming Li, Jing Ma, Wenlong Wang, Xu Yang, Kaizhong Luo. Mutation analysis of the ATP7B gene and genotype–phenotype correlation in Chinese patients with Wilson disease. BMC Gastroenterology 2021; 21(1) doi: 10.1186/s12876-021-01911-5
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| 3 |
Kok-Siong Poon, Karen Mei-Ling Tan, Evelyn Siew-Chuan Koay. Targeted next-generation sequencing of the ATP7B gene for molecular diagnosis of Wilson disease. Clinical Biochemistry 2016; 49(1-2) doi: 10.1016/j.clinbiochem.2015.10.003
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| 4 |
Li-Hua Wang, Ye-Qing Huang, Xuan Shang, Quan-Xi Su, Fu Xiong, Qing-Yun Yu, Hui-Ping Lin, Zhi-Sheng Wei, Ming-Fan Hong, Xiang-Min Xu. Mutation analysis of 73 southern Chinese Wilson's disease patients: identification of 10 novel mutations and its clinical correlation. Journal of Human Genetics 2011; 56(9) doi: 10.1038/jhg.2011.76
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| 5 |
Xinwen Huang, Dingwen Wu, Lin Zhu, Wenjun Wang, Rulai Yang, Jianbin Yang, Qunyan He, Bingquan Zhu, Ying You, Rui Xiao, Zhengyan Zhao. Application of a next-generation sequencing (NGS) panel in newborn screening efficiently identifies inborn disorders of neonates. Orphanet Journal of Rare Diseases 2022; 17(1) doi: 10.1186/s13023-022-02231-x
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| 6 |
Lei Wan, Chang-Hai Tsai, Chin-Moo Hsu, Chin-Chang Huang, Chih-Chao Yang, Chiu-Chu Liao, Chin-Ching Wu, Yu-An Hsu, Cheng-Chun Lee, Su-Ching Liu, Wei-De Lin, Fuu-Jen Tsai. Mutation Analysis and Characterization of Alternative Splice Variants of the Wilson Disease Gene ATP7B. Hepatology 2010; 52(5) doi: 10.1002/hep.23865
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| 7 |
New mutations and polymorphisms of the ATP7B gene in sporadic Wilson disease. European Journal of Medical Genetics 2014; 57(9) doi: 10.1016/j.ejmg.2014.04.016
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| 8 |
Sheng-Peng Diao, Ming-Fan Hong, Ye-Qing Huang, Zhi-Sheng Wei, Quan-Xi Su, Zhong-Xing Peng, Qing-Yun Yu, Ai-Qun Liu, Jin Chen, Li Hu. Identification and characterization of a novel splice-site mutation in the Wilson disease gene. Journal of the Neurological Sciences 2014; 345(1-2) doi: 10.1016/j.jns.2014.07.031
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| 9 |
Xin-Hua Li, Yi Lu, Yun Ling, Qing-Chun Fu, Jie Xu, Guo-Qing Zang, Feng Zhou, Yu De-Min, Yue Han, Dong-Hua Zhang, Qi-Ming Gong, Zhi-Meng Lu, Xiao-Fei Kong, Jian-She Wang, Xin-Xin Zhang. Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations. BMC Medical Genetics 2011; 12(1) doi: 10.1186/1471-2350-12-6
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| 10 |
Kui Li, Wei-Min Zhang, Sheng Lin, Lu Wen, Zi-Feng Wang, Dan Xie, Min Wei, Zheng-Qing Qiu, Yi Dai, Marie C M Lin, Hsiang-Fu Kung, Feng-Xia Yao. Mutational analysis of ATP7B in north Chinese patients with Wilson disease. Journal of Human Genetics 2013; 58(2) doi: 10.1038/jhg.2012.134
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| 11 |
Laimutis Kucinskas, Jolanta Jeroch, Astra Vitkauskiene, Raimundas Sakalauskas, Vitalija Petrenkiene, Vaidutis Kucinskas, Rima Naginiene, Hartmut Schmidt, Limas Kupcinskas. High frequency of the c.3207C>A (p.H1069Q) mutation in <italic>ATP7B</italic> gene of Lithuanian patients with hepatic presentation of Wilson’s disease. World Journal of Gastroenterology 2008; 14(38): 5876-5879 doi: 10.3748/wjg.14.5876
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| 12 |
Celia Badenas Orquin. Avances en el diagnóstico molecular de la enfermedad de Wilson. Gastroenterología y Hepatología 2011; 34(6) doi: 10.1016/j.gastrohep.2011.01.001
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| 13 |
Relu Cocoş, Alina Şendroiu, Sorina Schipor, Laurenţiu Camil Bohîlţea, Ionuţ Şendroiu, Florina Raicu, Bart Dermaut. Genotype-Phenotype Correlations in a Mountain Population Community with High Prevalence of Wilson’s Disease: Genetic and Clinical Homogeneity. PLoS ONE 2014; 9(6) doi: 10.1371/journal.pone.0098520
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| 14 |
Woong Choi, Seongkwang Cha, Kyoungmi Kim. Navigating the CRISPR/Cas Landscape for Enhanced Diagnosis and Treatment of Wilson’s Disease. Cells 2024; 13(14) doi: 10.3390/cells13141214
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| 15 |
Zhisheng Wei, Yeqing Huang, Aiqun Liu, Shengpeng Diao, Qingyun Yu, Zhongxing Peng, Mingfan Hong. Mutational characterization of ATP7B gene in 103 Wilson’s disease patients from Southern China. NeuroReport 2014; 25(14) doi: 10.1097/WNR.0000000000000216
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| 16 |
S Santhosh, RV Shaji, CE Eapen, V Jayanthi, S Malathi, P Finny, N Thomas, M Chandy, G Kurian, GM Chandy. Genotype phenotype correlation in Wilson’s disease within families-a report on four south Indian families. World Journal of Gastroenterology 2008; 14(29): 4672-4676 doi: 10.3748/wjg.14.4672
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