Case report: A novel cause of acute liver failure in children: A combination of human herpesvirus‐6 infection and homozygous mutation in <i>NBAS</i> gene-Reference-Cited by-同舟云学术

Case report: A novel cause of acute liver failure in children: A combination of human herpesvirus‐6 infection and homozygous mutation in NBAS gene

Published:2022-03-29 Issue:5 Volume:36 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:Clinical Laboratory Analysis

Author:

Cheng Ying¹,Xia Zhi¹,Huang Chengjiao¹,Xu Hui¹^ORCID

Affiliation:

1. Department of Pediatric Intensive Care Unit Maternal and Child Health Hospital of Hubei Province (Women and Children’s Hospital of Hubei Province) Wuhan China

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.24343

Reference20 articles.

1. Identification of the Neuroblastoma-amplified Gene Product as a Component of the Syntaxin 18 Complex Implicated in Golgi-to-Endoplasmic Reticulum Retrograde Transport

2. Identification and functional characterization of mutations in LPL gene causing severe hypertriglyceridaemia and acute pancreatitis

3. Whole exome sequencing identified a homozygous novel variant in CEP290 gene causes Meckel syndrome

4. Whole Exome Sequencing Identified a Novel Heterozygous Mutation in HMBS Gene in a Chinese Patient With Acute Intermittent Porphyria With Rare Type of Mild Anemia

5. Targeted next‐generation sequencing reveals two novel mutations of NBAS in a patient with infantile liver failure syndrome‐2;Wang J;Mol Med Rep,2018

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