Next generation sequencing reveals co-existence of hereditary spherocytosis and Dubin–Johnson syndrome in a Chinese gril: A case report-Reference-Cited by-同舟云学术

Next generation sequencing reveals co-existence of hereditary spherocytosis and Dubin–Johnson syndrome in a Chinese gril: A case report

Published:2019-10-26 Issue:20 Volume:7 Page:3303-3309
ISSN:2307-8960
Container-title:World Journal of Clinical Cases
language:
Short-container-title:WJCC

Author:

Li Yuan,Li Yang,Yang Yang,Yang Wen-Rui,Li Jian-Ping,Peng Guang-Xin,Song Lin,Fan Hui-Hui,Ye Lei,Xiong You-Zhen,Wu Zhi-Jie,Zhou Kang,Zhao Xin,Jing Li-Ping,Zhang Feng-Kui,Zhang Li

Publisher

Baishideng Publishing Group Inc.

Subject

General Medicine

Reference20 articles.

1. Severe jaundice due to coexistence of Dubin-Johnson syndrome and hereditary spherocytosis: A case report

2. ACMG clinical laboratory standards for next-generation sequencing

3. CHRONIC IDIOPATHIC JAUNDICE WITH UNIDENTIFIED PIGMENT IN LIVER CELLS

4. Mutations in the canilicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome

5. Genomic Structure of the Canalicular Multispecific Organic Anion–Transporter Gene (MRP2/cMOAT) and Mutations in the ATP-Binding–Cassette Region in Dubin-Johnson Syndrome

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1. Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report;BMC Pediatrics;2021-06-28

2. Neonatal Dubin–Johnson syndrome: biochemical parameters, characteristics, and genetic variants study;Pediatric Research;2021-05-28

3. Developing a gene panel for pharmacoresistant epilepsy: a review of epilepsy pharmacogenetics;Pharmacogenomics;2021-03