Familial NTCPD presenting with persistent hypercholanemia and co-existing with a series of novel heterozygous mutations - 08/08/24

Doi : 10.1016/j.clinre.2024.102444

Meifen Wang ^a,^{^{1
These authors contributed equally to the paper.}}, Lin Zhou ^b,^{^{1
These authors contributed equally to the paper.}}, Qian Zhang ^c, Juan Li ^d, Junchao Peng ^a, Rui Chen ^a, Qi Shao ^a, Zhongrui Bi ^a, Mingying Wang ^d,^⁎ , Jiwei Li ^e,^⁎
^a Department of Infectious Diseases, Kunming Children’s Hospital, The Affiliated Children’s Hospital of Kunming Medical University, Yunnan Province Clinical Research Center for Children's Health and Disease, Kunming, PR China
^b Department of Nutrition, Kunming Children’s Hospital, The Affiliated Children’s Hospital of Kunming Medical University, Yunnan Province Clinical Research Center for Children's Health and Disease, Kunming, PR China
^c Department of Clinical Laboratory, Kunming Children’s Hospital, The Affiliated Children’s Hospital of Kunming Medical University, Yunnan Province Clinical Research Center for Children's Health and Disease, Kunming, PR China
^d Department of Gastroenterology, Kunming Children’s Hospital, The Affiliated Children’s Hospital of Kunming Medical University, Yunnan Province Clinical Research Center for Children's Health and Disease, Kunming, PR China
^e Department of Pathology, Kunming Children's Hospital, The Affiliated Children's Hospital of Kunming Medical University, Yunnan Province Clinical Research Center for Children's Health and Disease, Kunming, PR China

^⁎Corresponding authors at: Kunming Children's Hospital, The Affiliated Children's Hospital of Kunming Medical University, Yunnan Province Clinical Research Center for Children's Health and Disease, 288 Qianxing Road, Kunming 650228, PR China.Kunming Children's Hospital, The Affiliated Children's Hospital of Kunming Medical University, Yunnan Province Clinical Research Center for Children's Health and Disease288 Qianxing RoadKunming650228PR China

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