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Structure modeling to function prediction of Uncharacterized Human Protein C15orf41
The dyserythropoietic anemia disease is a genetic disorder of erythropoiesis characterized by morphological abnormalities of erythroblasts. This is caused by human gene C15orf41 mutation. The uncharacterized C15orf41 protein is involved in the formation of a functional complex structure. The unchara...
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| Publié dans: | Bioinformation |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Biomedical Informatics
2018
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6077826/ https://ncbi.nlm.nih.gov/pubmed/30108417 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6026/97320630014206 |
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