Molecular basis of Diamond–Blackfan anemia: structure and function analysis of RPS19

Diamond–Blackfan anemia (DBA) is a rare congenital disease linked to mutations in the ribosomal protein genes rps19, rps24 and rps17. It belongs to the emerging class of ribosomal disorders. To understand the impact of DBA mutations on RPS19 function, we have solved the crystal structure of RPS19 fr...

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Detalles Bibliográficos
Autores principales: Gregory, Lynn A., Aguissa-Touré, Almass-Houd, Pinaud, Noël, Legrand, Pierre, Gleizes, Pierre-Emmanuel, Fribourg, Sébastien
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Structural Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034476/
https://www.ncbi.nlm.nih.gov/pubmed/17726054
http://dx.doi.org/10.1093/nar/gkm626

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034476/
https://www.ncbi.nlm.nih.gov/pubmed/17726054
http://dx.doi.org/10.1093/nar/gkm626

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