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Cockayne Syndrome: The many challenges and approaches to understand a multifaceted disease

The striking and complex phenotype of Cockayne syndrome (CS) patients combines progeria-like features with developmental deficits. Since the establishment of the in vitro culture of skin fibroblasts derived from patients with CS in the 1970s, significant progress has been made in the understanding o...

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Bibliografske podrobnosti
izdano v:Genet Mol Biol
Main Authors: Vessoni, Alexandre Teixeira, Guerra, Camila Chaves Coelho, Kajitani, Gustavo Satoru, Nascimento, Livia Luz Souza, Garcia, Camila Carrião Machado
Format: Artigo
Jezik:Inglês
Izdano: Sociedade Brasileira de Genética 2020
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7250278/
https://ncbi.nlm.nih.gov/pubmed/32453336
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/1678-4685-GMB-2019-0085
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