Systematic analysis of a mitochondrial disease‐causing ND6 mutation in mitochondrial deficiency-Reference-Cited by-同舟云学术

Systematic analysis of a mitochondrial disease‐causing ND6 mutation in mitochondrial deficiency

Published:2020-03-12 Issue:5 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Chen Deyu¹,Zhao Qiongya²^ORCID,Xiong Jingting³,Lou Xiaoting¹,Han Qinxia¹,Wei Xiujuan¹,Xie Jie¹,Li Xueyun¹,Zhou Huaibin¹,Shen Lijun¹,Yang Yanling⁴,Fang Hezhi¹,Lyu Jianxin¹²^ORCID

Affiliation:

1. Key Laboratory of Laboratory Medicine Ministry of Education Zhejiang Provincial Key Laboratory of Medical Genetics College of Laboratory Medicine and Life sciences Wenzhou Medical University Wenzhou China

2. Zhejiang Provincial People's Hospital Affiliated People's Hospital of Hangzhou Medical College College of Laboratory Medicine Hangzhou Medical College Hangzhou China

3. Department of Laboratory Medicine Liyuan HospitalTongji Medical CollegeHuazhong University of Science and Technology Wuhan China

4. Department of Pediatrics Peking University First HospitalPeking University Beijing China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1199

Reference62 articles.

1. Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency