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Mutations affecting mRNA splicing are the most common molecular defect in patients with familial hemophagocytic lymphohistiocytosis type 3.

Authors
Type
Published Article
Journal
Haematologica
1592-8721
Publisher
Ferrata Storti Foundation
Publication Date
Volume
93
Issue
7
Pages
1086–1090
Identifiers
DOI: 10.3324/haematol.12622
PMID: 18492689
Source
Medline

Abstract

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