Neonatal liver failure and haemophagocytic lymphohistiocytosis caused by a new perforin mutation
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2009.01647.x/fullpdf
Reference12 articles.
1. Acute liver failure in neonates;Dhawan;Early Hum Dev,2005
2. Acute liver failure in children: the first 348 patients in the pediatric acute liver failure study group;Squires;J Pediatr,2006
3. Cell-mediated cytotoxicity in Down-syndrome: impairment of allogeneic mixed lymphocyte reaction, NK and N-like activities;Montagna;Eur J Pediatr,1988
4. Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis;Göransdotter Ericson;Am J Hum Genet,2001
5. Perforin gene defects in familial hemophagocytic lymphohistiocytosis;Stepp;Science,1999
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