UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis

Published 2009 View Full Article

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Title
UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis
Authors
Keywords
-
Journal
HAEMATOLOGICA
Volume 95, Issue 4, Pages 622-626
Publisher
Ferrata Storti Foundation (Haematologica)
Online
2009-12-17
DOI
10.3324/haematol.2009.016949

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