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Congenital neutropenia: diagnosis, molecular bases and patient management
The term congenital neutropenia encompasses a family of neutropenic disorders, both permanent and intermittent, severe (<0.5 G/l) or mild (between 0.5-1.5 G/l), which may also affect other organ systems such as the pancreas, central nervous system, heart, muscle and skin. Neutropenia can lead to...
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| Päätekijät: | , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3127744/ https://ncbi.nlm.nih.gov/pubmed/21595885 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-26 |
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