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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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Main Authors: Gregory, Lynn A., Aguissa-Touré, Almass-Houd, Pinaud, Noël, Legrand, Pierre, Gleizes, Pierre-Emmanuel, Fribourg, Sébastien
格式: Artigo
語言:Inglês
出版: Oxford University Press 2007
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2034476/
https://ncbi.nlm.nih.gov/pubmed/17726054
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkm626
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