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Genetic Diagnosis of Cockayne Syndrome

Researchers from the University of Strasbourg investigated whether defective transcription of ATF3 responsive genes is a marker for Cockayne Syndrome (CS).

Detalles Bibliográficos
Autor principal: Patel, Rifali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pediatric Neurology Briefs Publishers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713631/
https://www.ncbi.nlm.nih.gov/pubmed/33281429
http://dx.doi.org/10.15844/pedneurbriefs-34-9
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author Patel, Rifali
author_facet Patel, Rifali
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description Researchers from the University of Strasbourg investigated whether defective transcription of ATF3 responsive genes is a marker for Cockayne Syndrome (CS).
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spelling pubmed-77136312020-12-04 Genetic Diagnosis of Cockayne Syndrome Patel, Rifali Pediatr Neurol Briefs Genetic Disorders Researchers from the University of Strasbourg investigated whether defective transcription of ATF3 responsive genes is a marker for Cockayne Syndrome (CS). Pediatric Neurology Briefs Publishers 2020-12-02 /pmc/articles/PMC7713631/ /pubmed/33281429 http://dx.doi.org/10.15844/pedneurbriefs-34-9 Text en Copyright: © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genetic Disorders
Patel, Rifali
Genetic Diagnosis of Cockayne Syndrome
title Genetic Diagnosis of Cockayne Syndrome
title_full Genetic Diagnosis of Cockayne Syndrome
title_fullStr Genetic Diagnosis of Cockayne Syndrome
title_full_unstemmed Genetic Diagnosis of Cockayne Syndrome
title_short Genetic Diagnosis of Cockayne Syndrome
title_sort genetic diagnosis of cockayne syndrome
topic Genetic Disorders
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713631/
https://www.ncbi.nlm.nih.gov/pubmed/33281429
http://dx.doi.org/10.15844/pedneurbriefs-34-9
work_keys_str_mv AT patelrifali geneticdiagnosisofcockaynesyndrome