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Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?

作者信息

Warang Prashant, Devendra Rati, D'Silva Selma, Chiddarwar Ashish, Kedar Prabhakar, Ghosh Kanjaksha, Colah Roshan, Mukherjee Malay B

机构信息

Department of Haematogenetics, National Institute of Immunohaematology, Indian Council of Medical Research, K.E.M. Hospital Campus, 13th floor, NMS building, Parel, Mumbai, 400012, India.

出版信息

Ann Hematol. 2015 Jan;94(1):169-71. doi: 10.1007/s00277-014-2123-z. Epub 2014 Jun 20.

DOI:10.1007/s00277-014-2123-z
PMID:24947795
Abstract
摘要

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Association of gallstone and polymorphisms of and in patients with hepatitis B virus-related liver failure.乙型肝炎病毒相关肝衰竭患者胆结石与[具体基因1]和[具体基因2]多态性的关联
Open Med (Wars). 2022 Sep 6;17(1):1455-1465. doi: 10.1515/med-2022-0549. eCollection 2022.
2
Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.韩国遗传性球形红细胞增多症的多基因靶序列分子诊断:与渗透脆性试验和球形红细胞存在相匹配。
Orphanet J Rare Dis. 2019 May 23;14(1):114. doi: 10.1186/s13023-019-1070-0.
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Polymorphisms in Gene Predispose South Indians to Pigmentous Gallstones.
基因多态性使南印度人易患色素性胆结石。
J Clin Exp Hepatol. 2016 Sep;6(3):216-223. doi: 10.1016/j.jceh.2016.08.004. Epub 2016 Aug 30.