Insertion of LINE-1 Retrotransposon Inducing Exon Inversion Causes a Rotor Syndrome Phenotype-Reference-Cited by-同舟云学术

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Insertion of LINE-1 Retrotransposon Inducing Exon Inversion Causes a Rotor Syndrome Phenotype

Published:2020-01-31 Issue: Volume:10 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Zhou Donghu,Qi Saiping,Zhang Wei,Wu Lina,Xu Anjian,Li Xiaojin,Zhang Bei,Li Yanmeng,Jia Siyu,Wang Hejing,Jia Jidong,Ou Xiaojuan,Huang Jian,You Hong

Funder

National Natural Science Foundation of China

Beijing Postdoctoral Research Foundation

Publisher

Frontiers Media SA

Subject

Genetics (clinical),Genetics,Molecular Medicine

Reference25 articles.

1. Comprehensive scanning mutagenesis of human retrotransposon LINE-1 identifies motifs essential for function;Adney;Genetics.,2019

2. Transposable elements in cancer;Burns;Nat. Rev. Cancer,2017

3. LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease: mutation detection bias and multiple mechanisms of target gene disruption;Chen;J. Biomed. Biotechnol.,2006

4. The impact of retrotransposons on human genome evolution;Cordaux;Nat. Rev. Genet.,2009

5. Mutation surveyor: an in silico tool for sequencing analysis;Dong;Methods Mol. Biol.,2011

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1. The utility of hierarchical genetic testing in paediatric liver disease;Liver International;2022-03-21

2. Phenotypic and genotypic analysis of children with methylmalonic academia: A single-center study in China and a recent literature review;Clinica Chimica Acta;2021-11

3. Intronic LINE-1 insertion in SLCO1B3 as a highly prevalent cause of rotor syndrome in East Asian population;Journal of Human Genetics;2021-08-05

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