NovelHMGCS2pathogenic variants in a Chinese family with mitochondrial 3‐hydroxy‐3‐methylglutaryl‐CoA synthase deficiency-Reference-Cited by-同舟云学术

NovelHMGCS2pathogenic variants in a Chinese family with mitochondrial 3‐hydroxy‐3‐methylglutaryl‐CoA synthase deficiency

Published:2019-06 Issue:2 Volume:3 Page:86-90
ISSN:2574-2272
Container-title:PEDIATRIC INVESTIGATION
language:en
Short-container-title:Pediatr Invest

Author:

Zhang Pengfei¹,Hu Xuyun²³,Guo Ruolan²³,Guo Jun²³,Li Wei²³,Qian Suyun¹,Hao Chanjuan²³,Liu Jun¹

Affiliation:

1. Department of Pediatric Intensive Care Unit Beijing Children's Hospital Capital Medical University; National Center for Children's Health Beijing 100045 China

2. Beijing Key Laboratory for Genetics of Birth Defects Beijing Pediatric Research Institute; MOE Key Laboratory of Major Diseases in Children; Genetics and Birth Defects Control Center Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China

3. Henan Key Laboratory of Pediatric Inherited & Metabolic Diseases Henan Children's Hospital Zhengzhou Hospital of Beijing Children's Hospital Zhengzhou China

Funder

The Ministry of Science and Technology of China

Beijing Municipal Science and Technology Commission Foundation

Beijing Municipal Commission of Health and Family Planning Foundation

Beijing Municipal Administration of Hospitals Foundation

Publisher

Wiley

Subject

Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ped4.12130

Reference15 articles.