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Immunofluorescence studies to dissect the impact of Cockayne syndrome A alterations on the protein interaction and cellular localization
BACKGROUND: Cockayne syndrome (CS), which was discovered by Alfred Cockayne nearly 75 years ago, is a rare autosomal recessive disorder characterized by growth failure, neurological dysfunction, premature aging, and other clinical features including microcephaly, ophthalmologic abnormalities, dental...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208330/ https://www.ncbi.nlm.nih.gov/pubmed/34132928 http://dx.doi.org/10.1186/s43141-021-00190-7 |