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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...

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Hlavní autoři: Ward, Alister C., Dale, David C.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2009
Témata:
On-line přístup: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
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