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Genetic Diagnosis of Cockayne Syndrome Cover

Genetic Diagnosis of Cockayne Syndrome

By:   
Open Access
|Dec 2020

References

  1. Epanchintsev A Rauschendorf MA Costanzo F Calmels N Obringer C Sarasin A Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome Sci Rep 2020 Jan 10 1 1105 https://doi.org/10.1038/s41598-020-57999-4 31980658
  2. Karikkineth AC Scheibye-Knudsen M Fivenson E Croteau DL Bohr VA Cockayne syndrome: clinical features, model systems and pathways Ageing Res Rev 2017 Jan 33 3 17 https://doi.org/10.1016/j.arr.2016.08.002 27507608
  3. Kleijer WJ van der Sterre ML Garritsen VH Raams A Jaspers NG Prenatal diagnosis of the Cockayne syndrome: survey of 15 years experience Prenat Diagn 2006 Oct 26 10 980 4 https://doi.org/10.1002/pd.1541 16941719
Language: English
Page range: 9 - 9
Submitted on: Mar 1, 2020
Accepted on: Nov 29, 2020
Published on: Dec 2, 2020
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services

© 2020 Rifali Patel, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.