Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. (Q33376697)
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Language | Label | Description | Also known as |
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English | Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. |
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Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations (English)
A Trizzino
U zur Stadt
I Ueda
G Janka
E Ishii
K Beutel
J Sumegi
S Cannella
D Pende
A Mian
G Griffiths
A Santoro
A Filipovich
M Aricò
Histiocyte Society HLH Study group
14 September 2007