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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).
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Pediatric Neurology Briefs Publishers
2020
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| 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 |