Neurologic Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: Aicardi–Goutières Syndrome and Beyond-Reference-Cited by-同舟云学术

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Neurologic Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: Aicardi–Goutières Syndrome and Beyond

Published:2016-09-19 Issue:06 Volume:47 Page:355-360
ISSN:0174-304X
Container-title:Neuropediatrics
language:en
Short-container-title:Neuropediatrics

Author:

Crow Yanick¹,Livingston John²

Affiliation:

1. Laboratory of Neurogenetics and Neuroinflammation, Institut Imagine, Paris Descartes–Sorbonne Paris Cité University, Paris, France

2. Department of Paediatric Neurology, Leeds Teaching Hospitals NHS Trust, Leeds General Infirmary, Leeds, United Kingdom

Publisher

Georg Thieme Verlag KG

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0036-1592307.pdf

Cited by 138 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Single gene defects and autoinflammation;Dubois' Lupus Erythematosus and Related Syndromes;2025

2. Second generation lethality in RNAseH2a knockout zebrafish;Nucleic Acids Research;2024-09-01

3. A case of severe Aicardi–Goutières syndrome with a homozygous RNASEH2B intronic variant;Human Genome Variation;2024-08-26

4. Neurophenotype and genetic analysis of children with Aicardi‐Goutières syndrome in China;Pediatric Investigation;2024-05-30

5. Systematic analysis of genotype-phenotype variability in siblings with Aicardi Goutières Syndrome (AGS);Molecular Genetics and Metabolism;2024-05

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