Computational Studies of the Structural Basis of Human RPS19 Mutations Associated With Diamond-Blackfan Anemia

Diamond-Blackfan Anemia (DBA) is an inherited rare disease characterized with severe pure red cell aplasia, and it is caused by the defective ribosome biogenesis stemming from the impairment of ribosomal proteins. Among all DBA-associated ribosomal proteins, RPS19 affects most patients and carries m...

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Detalles Bibliográficos
Autores principales: An, Ke, Zhou, Jing-Bo, Xiong, Yao, Han, Wei, Wang, Tao, Ye, Zhi-Qiang, Wu, Yun-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8181406/
https://www.ncbi.nlm.nih.gov/pubmed/34108988
http://dx.doi.org/10.3389/fgene.2021.650897

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8181406/
https://www.ncbi.nlm.nih.gov/pubmed/34108988
http://dx.doi.org/10.3389/fgene.2021.650897

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