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Molecular mechanisms of neutrophil dysfunction in glycogen storage disease type Ib
Glycogen storage disease type Ib (GSD-Ib) is an autosomal-recessive syndrome characterized by neutropenia and impaired glucose homeostasis resulting from a deficiency in the glucose-6-phosphate (G6P) transporter (G6PT). The underlying cause of GSD-Ib neutropenia is an enhanced neutrophil apoptosis,...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Hematology
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4007611/ https://ncbi.nlm.nih.gov/pubmed/24565827 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2013-05-502435 |
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