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Incomplete splicing of neutrophil-specific genes affects neutrophil development in a zebrafish model of poikiloderma with neutropenia

Poikiloderma with neutropenia (PN) is a rare inherited disorder characterized by poikiloderma, facial dysmorphism, pachyonychia, short stature and neutropenia. The molecular testing of PN patients has identified mutations in the C16orf57 gene, which encodes a protein referred to as USB1 (U Six Bioge...

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Detalhes bibliográficos
Publicado no:RNA Biol
Main Authors: Patil, Prakash, Uechi, Tamayo, Kenmochi, Naoya
Formato: Artigo
Idioma:Inglês
Publicado em: Taylor & Francis 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4615382/
https://ncbi.nlm.nih.gov/pubmed/25849198
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15476286.2015.1017240
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