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ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Issue 10
Oct.  2018
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A case of congenital hepatic fibrosis with lgG4-related disease

DOI: 10.3969/j.issn.1001-5256.2018.10.026
  • Published Date: 2018-10-20
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    [2]WARD CJ, YUAN D, MASYUK TV, et al.Cellular and subcellular localization of the ARPKD protein;fibrocystin is expressed on primary cilia[J].Hum Mol Genet, 2003, 12 (20) :2703-2710.
    [3]ZHANG MZ, MAI W, LI C, et al.PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells[J].Proc Natl Acad Sci U S A, 2004, 101 (8) :2311-2316.
    [4]ONUCHIC LF, FURU L, NAGASAWA Y, et al.PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats[J].Am J Hum Genet, 2002, 70 (5) :1305-1317.
    [5]WARD CJ, HOGAN MC, ROSSETTI S, et al.The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein[J].Nat Genet, 2002, 30 (3) :259-269.
    [6]GUNAY-AYGUN M, TUCHMAN M, FONT-MONTGOMERYE, et al.PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic kidney disease and congenital hepatic fibrosis[J].Mol Genet Metab, 2010, 99 (2) :160-173.
    [7]FENG MS, MA WB, TANG SH, et al.Pathogenesis of congenital hepatic fibrosis and current status of its diagnosis and treatment[J].J Clin Hepatol, 2017, 33 (3) :553-557. (in Chinese) 冯茂森, 马文斌, 汤善宏, 等.先天性肝纤维化的发病机制及诊治现状[J].临床肝胆病杂志, 2017, 33 (3) :553-557.
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    [10]CHENG ZL, WANG YM.Research progress of Ig G4 associated cholangitis[J].Chin Hepatol, 2015, 20 (9) :721-722, 732. (in Chinese) 程智玲, 王宇明.Ig G4相关性胆管炎的研究进展[J].肝脏, 2015, 20 (9) :721-722, 732.
    [11]ZHU XF, ZOU DW.Research progress of Ig G4 related digestive diseases[J].Chin J Pancreatol, 2014, 14 (1) :57-61. (in Chinese) 朱晓斐, 邹多武.Ig G4相关性消化疾病的研究进展[J].中华胰腺病杂志, 2014, 14 (1) :57-61.
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    [15]TANG RJ, LIU ZW, SU HB, et al.The clinical features analysis of48 cases of congenital hepatic fibrosis[J].Chin Hepatol, 2013, 18 (2) :75-76. (in Chinese) 汤汝佳, 刘振文, 苏海滨, 等.先天性肝纤维化48例临床特点分析[J].肝脏, 2013, 18 (2) :75-76.
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