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Dive into the research topics of 'STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5'. Together they form a unique fingerprint.- Sort by
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Valentina Cetica, Alessandra Santoro, Kimberly C. Gilmour, Elena Sieni, Karin Beutel, Daniela Pende, Stefania Marcenaro, Florian Koch, Samantha Grieve, Rachel Wheeler, Fang Zhao, Udo Zur Stadt, Gillian M. Griffiths, Maurizio Aricò
Research output: Contribution to journal › Article › peer-review