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Analysis of cilia dysfunction phenotypes in zebrafish embryos depleted of Origin recognition complex factors
Meier–Gorlin syndrome (MGS) is a rare, congenital primordial microcephalic dwarfism disorder. MGS is caused by genetic variants of components of the origin recognition complex (ORC) consisting of ORC1–6 and the pre-replication complex, which together enable origin firing and hence genome replication...
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| Publicat a: | Eur J Hum Genet |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer International Publishing
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6461852/ https://ncbi.nlm.nih.gov/pubmed/30696958 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-019-0338-0 |
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