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l-leucine partially rescues translational and developmental defects associated with zebrafish models of Cornelia de Lange syndrome
Cohesinopathies are human genetic disorders that include Cornelia de Lange syndrome (CdLS) and Roberts syndrome (RBS) and are characterized by defects in limb and craniofacial development as well as mental retardation. The developmental phenotypes of CdLS and other cohesinopathies suggest that mutat...
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| 發表在: | Hum Mol Genet |
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| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Oxford University Press
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4351377/ https://ncbi.nlm.nih.gov/pubmed/25378554 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu565 |
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