Benign Recurrent Intrahepatic Cholestasis
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Last Posted: Mar 04, 2023
- Genetic contribution of ABCC2 to Dubin-Johnson syndrome and inherited cholestatic disorders.
Corpechot Christophe, et al. Liver international : official journal of the International Association for the Study of the Liver 2019 0 (1) 163-174 - Genetic Causes of Liver Disease: When to Suspect a Genetic Etiology, Initial Lab Testing, and the Basics of Management.
Schonfeld Emily A et al. The Medical clinics of North America 2019 Nov 103(6) 991-1003 - Clinical phenotype and molecular analysis of a homozygous ABCB11 mutation responsible for progressive infantile cholestasis.
Imagawa Kazuo, et al. Journal of human genetics 2018 3 - Genetic Testing in Liver Disease: What to Order, in Whom, and When.
Schonfeld Emily A et al. Clinics in liver disease 2017 Nov 21(4) 673-686 - Molecular Genetic Dissection and Neonatal/Infantile Intrahepatic Cholestasis Using Targeted Next-Generation Sequencing.
Togawa Takao, et al. The Journal of pediatrics 2016 2 - Benign recurrent intrahepatic cholestasis
From NCATS Genetic and Rare Diseases Information Center - Benign recurrent intrahepatic cholestasis 1
From NCATS Genetic and Rare Diseases Information Center - Benign recurrent intrahepatic cholestasis 2
From NCATS Genetic and Rare Diseases Information Center - Diagnosis of BSEP/ABCB11 mutations in Asian patients with cholestasis using denaturing high performance liquid chromatography.
Chen Huey-Ling, et al. The Journal of pediatrics 2008 12 (6) 825-32 - ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy.
Müllenbach R, et al. Gut 2005 6 (6) 829-34
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- Page last reviewed:Feb 1, 2024
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