» Articles » PMID: 37405491

A Child with Chronic Kidney Disease and Hepatic Dysfunction: Answers

Overview
Journal Pediatr Nephrol
Specialties Nephrology
Pediatrics
Date 2023 Jul 5
PMID 37405491
Authors
Affiliations
Soon will be listed here.
References
1.
Turnpenny P, Ellard S . Alagille syndrome: pathogenesis, diagnosis and management. Eur J Hum Genet. 2011; 20(3):251-7. PMC: 3283172. DOI: 10.1038/ejhg.2011.181. View

2.
Li L, Krantz I, Deng Y, Genin A, Banta A, Collins C . Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. Nat Genet. 1997; 16(3):243-51. DOI: 10.1038/ng0797-243. View

3.
Oda T, Elkahloun A, Pike B, Okajima K, Krantz I, Genin A . Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nat Genet. 1997; 16(3):235-42. DOI: 10.1038/ng0797-235. View

4.
Crosnier C, Driancourt C, Raynaud N, Dhorne-Pollet S, Pollet N, Bernard O . Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome. Gastroenterology. 1999; 116(5):1141-8. DOI: 10.1016/s0016-5085(99)70017-x. View

5.
Saleh M, Kamath B, Chitayat D . Alagille syndrome: clinical perspectives. Appl Clin Genet. 2016; 9:75-82. PMC: 4935120. DOI: 10.2147/TACG.S86420. View