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The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNA

Shwachman-Diamond syndrome (SDS) is an autosomal recessive disorder characterized by bone marrow failure, exocrine pancreatic dysfunction, and leukemia predisposition. Mutations in the SBDS gene are identified in most patients with SDS. SBDS encodes a highly conserved protein of unknown function. Da...

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Detalhes bibliográficos
Main Authors: Ganapathi, Karthik A., Austin, Karyn M., Lee, Chung-Sheng, Dias, Anusha, Malsch, Maggie M., Reed, Robin, Shimamura, Akiko
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2007
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1975835/
https://ncbi.nlm.nih.gov/pubmed/17475909
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2007-02-075184
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