ATP8B1, ABCB11, and ABCB4 Genes Defects: Novel Mutations Associated with Cholestasis with Different Phenotypes and Outcomes-Reference-Cited by-同舟云学术

ATP8B1, ABCB11, and ABCB4 Genes Defects: Novel Mutations Associated with Cholestasis with Different Phenotypes and Outcomes

Published:2021-09 Issue: Volume:236 Page:113-123.e2
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Al-Hussaini Abdulrahman,Lone Khurram,Bashir Muhammed Salman,Alrashidi Sami,Fagih Mosa,Alanazi Alanoud,AlYaseen Salem,Almayouf Abdulaziz,Alruwaithi Muhanad,Asery Ali

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference17 articles.

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2. Differences in presentation and progression between severe FIC1 and BSEP deficiencies;Pawlikowska;J Hepatol,2010

3. Clinical features and genotype-phenotype correlations in children with progressive familial intrahepatic cholestasis type 3 related to ABCB4 mutations;Colombo;J Pediatr Gastroenterol Nutr,2011

4. The wide spectrum of multidrug resistance 3 deficiency: from neonatal cholestasis to cirrhosis of adulthood;Jacquemin;Gastroenterology,2001

5. Progressive familial intrahepatic cholestasis;Bull;Clin Liver Dis,2018

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