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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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Detalles Bibliográficos
Autores principales:	Ahmed, Md. Shakil, Shahjaman, Md., Kabir, Enamul, Kamruzzaman, Md.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Biomedical Informatics 2018
Materias:	Hypothesis
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077826/ https://www.ncbi.nlm.nih.gov/pubmed/30108417 http://dx.doi.org/10.6026/97320630014206

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