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An ever-changing landscape in Roberts syndrome biology: Implications for macromolecular damage
Roberts syndrome (RBS) is a rare developmental disorder that can include craniofacial abnormalities, limb malformations, missing digits, intellectual disabilities, stillbirth, and early mortality. The genetic basis for RBS is linked to autosomal recessive loss-of-function mutation of the establishme...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Public Library of Science
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774850/ https://www.ncbi.nlm.nih.gov/pubmed/33382686 http://dx.doi.org/10.1371/journal.pgen.1009219 |