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Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identified.
Xiao, Zhongyan; Yang, Yuan; Huang, Hui; Tang, Haiyan; Liu, Liqun; Tang, Jianguang; Shi, Xiaoliu.
Affiliation
  • Xiao Z; Department of Medical Genetics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China.
  • Yang Y; Department of Gastroenterology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China.
  • Huang H; Department of Medical Genetics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China.
  • Tang H; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), ICU, Peking University Cancer Hospital & Institute, Beijing, 100142, People's Republic of China.
  • Liu L; Department of Medical Genetics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China.
  • Tang J; Department of Medical Genetics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China.
  • Shi X; Department of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China.
Mol Genet Genomic Med ; 9(9): e1735, 2021 09.
Article in En | MEDLINE | ID: mdl-34324271
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Copper-Transporting ATPases / Hepatolenticular Degeneration Limits: Humans Country/Region as subject: Asia Language: En Journal: Mol Genet Genomic Med Year: 2021 Document type: Article Affiliation country: China Country of publication: United States
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Copper-Transporting ATPases / Hepatolenticular Degeneration Limits: Humans Country/Region as subject: Asia Language: En Journal: Mol Genet Genomic Med Year: 2021 Document type: Article Affiliation country: China Country of publication: United States