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Ribosome defects in disorders of erythropoiesis

Over the past decade, genetic lesions that cause ribosome dysfunction have been identified in both congenital and acquired human disorders. These discoveries have established a new category of disorders, known as ribosomopathies, in which the primary pathophysiology is related to impaired ribosome f...

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Hlavní autoři: Narla, Anupama, Hurst, Slater N., Ebert, Benjamin L.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2011
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3689295/
https://ncbi.nlm.nih.gov/pubmed/21279816
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12185-011-0776-0
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