Unusual functional manifestations of a novel STX11 frameshift mutation in two infants with familial hemophagocytic lymphohistiocytosis type 4 (FHL4)
Year: 2010
Type: article
Study design: Case Report
Source: Pediatric Blood & Cancer
DOI: 10.1002/pbc.22676
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W1990817138
