Congenital neutropenia: diagnosis, molecular bases and patient management
<p>Abstract</p> <p>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, musc...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2011-05-01
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Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | http://www.ojrd.com/content/6/1/26 |