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Conserved missense variant in ALDH1A3 ortholog impairs fecundity in C. elegans
Accumulating evidence demonstrates that mutations in ALDH1A3 (the aldehyde dehydrogenase 1 family, member A3) are associated with developmental defects. The ALDH1A3 enzyme catalyzes retinoic acid biosynthesis and is essential to patterning and neuronal differentiation in the development of embryonic...
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| Publicado no: | MicroPubl Biol |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Caltech Library
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7812383/ https://ncbi.nlm.nih.gov/pubmed/33474529 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.17912/micropub.biology.000357 |
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