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3 articles related to "Rnaseh1"

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Articles

Case Report

Published on 31 May 2022

Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions

in Genetics of Common and Rare Diseases

Arianna Manini
Leonardo Caporali
Megi Meneri
Simona Zanotti
Daniela Piga
Ignazio Giuseppe Arena
Stefania Corti
Antonio Toscano
Giacomo Pietro Comi
Olimpia Musumeci

Frontiers in Genetics

doi 10.3389/fgene.2022.906667

3,199 views
6 citations

Original Research

Published on 31 Jan 2020

RNase H1 Regulates Mitochondrial Transcription and Translation via the Degradation of 7S RNA

in Epigenomics and Epigenetics

Aurelio Reyes
Joanna Rusecka
Katarzyna Tońska
Massimo Zeviani

Frontiers in Genetics

doi 10.3389/fgene.2019.01393

8,003 views
16 citations

Original Research

Published on 14 Jun 2019

Identification and Characterization of New RNASEH1 Mutations Associated With PEO Syndrome and Multiple Mitochondrial DNA Deletions

in Genetics of Common and Rare Diseases

Lidia Carreño-Gago
Cora Blázquez-Bermejo
Jordi Díaz-Manera
Yolanda Cámara
Eduard Gallardo
Ramon Martí
Javier Torres-Torronteras
Elena García-Arumí

Frontiers in Genetics

doi 10.3389/fgene.2019.00576

5,550 views
12 citations