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

doi:10.1016/j.clinre.2024.102444

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

Clinics and research in hepatology and gastroenterology - 1 Oct 2024

Wang Meifen, Zhou Lin, Zhang Qian, Li Juan, Peng Junchao, Chen Rui, Shao Qi, Bi Zhongrui, Wang Mingying, Li Jiwei

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Share to Amyloid Neuropathies, Familial
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PMID: 39111575
DOI: 10.1016/j.clinre.2024.102444

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