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Genetic and molecular diagnosis of severe congenital neutropenia
PURPOSE OF REVIEW: Severe congenital neutropenia has been a well-known haematological condition for over 50 years. Over this long period of time, the variable genetic etiology and associated sequelae of the disease have been ascertained, and successful treatment strategies developed. Over the last 2...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2009
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2720320/ https://ncbi.nlm.nih.gov/pubmed/19057199 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MOH.0b013e32831952de |
| Etiketak: |
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