Journal
Genetics and Molecular Biology
Publication Date
1-1-2020
Volume
43
Issue
1 suppl. 1
First Page
e20190085
Document Type
Open Access Publication
DOI
10.1590/1678-4685-GMB-2019-0085
Rights and Permissions
Vessoni, Alexandre Teixeira, Guerra, Camila Chaves Coelho, Kajitani, Gustavo Satoru, Nascimento, Livia Luz Souza, & Garcia, Camila Carrião Machado. (2020). Cockayne Syndrome: The many challenges and approaches to understand a multifaceted disease. Genetics and Molecular Biology, 43(1, Suppl. 1), e20190085. Epub May 20, 2020.https://doi.org/10.1590/1678-4685-gmb-2019-0085 License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited.
Recommended Citation
Vessoni, Alexandre Teixeira; Guerra, Camila Chaves Coelho; Kajitani, Gustavo Satoru; Nascimento, Livia Luz Souza; and Garcia, Camila Carrião Machado, "Cockayne Syndrome: The many challenges and approaches to understand a multifaceted disease." Genetics and Molecular Biology. 43, 1 suppl. 1. e20190085 (2020).
https://digitalcommons.wustl.edu/open_access_pubs/9902
Table S1- Homozygous and heterozygous ERCC6 (CSB) mutations and their effects on patients phenotype.
1415-4757-GMB-43-1-s1-e20190085-suppl2.pdf (242 kB)
Table S2- Homozygous and heterozygous ERCC8 (CSA) mutations and their effects on patients phenotype.