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64. Whole-Genome Sequencing Reveals Large ATP8B1 Deletion/Duplications as Second Mutations Missed by Exome-Based Sequencing. Yang Y; Zhang J; Li LT; Qiu YL; Gong JY; Zhang MH; Li CH; Wang JS J Mol Diagn; 2021 Nov; 23(11):1491-1499. PubMed ID: 34543749 [TBL] [Abstract][Full Text] [Related]
65. [Progressive familial intrahepatic cholestasis related to mutation of the TJP2 gene: recent advances]. Zhang J; Yu H Zhonghua Gan Zang Bing Za Zhi; 2016 Jan; 24(1):78-80. PubMed ID: 26983395 [TBL] [Abstract][Full Text] [Related]
66. Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22. Arnell H; Nemeth A; Annerén G; Dahl N Hum Genet; 1997 Sep; 100(3-4):378-81. PubMed ID: 9272158 [TBL] [Abstract][Full Text] [Related]
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73. Cholestasis Due to USP53 Deficiency. Bull LN; Ellmers R; Foskett P; Strautnieks S; Sambrotta M; Czubkowski P; Jankowska I; Wagner B; Deheragoda M; Thompson RJ J Pediatr Gastroenterol Nutr; 2021 May; 72(5):667-673. PubMed ID: 33075013 [TBL] [Abstract][Full Text] [Related]
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76. Cracking the genetic code for benign recurrent and progressive familial intrahepatic cholestasis. Oude Elferink RP; van Berge Henegouwen GP J Hepatol; 1998 Aug; 29(2):317-20. PubMed ID: 9722216 [No Abstract] [Full Text] [Related]