Cerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndrome
Type II Griscelli Syndrome (GS) is caused by a mutation in the RAB27A gene and usually manifests with silvery-gray hair, immune deficiency and the development of hemophagocytic lymphohistiocytosis (HLH). A hematopoietic stem cell transplantation is the curative treatment for HLH and reduced-intensit...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
Galenos Yayinevi,
2019-09-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |