A functional analysis of the putative polymorphisms A91V and N252S and 22 missense perforin mutations associated with familial hemophagocytic …
I Voskoboinik, MC Thia, JA Trapani - Blood, 2005 - ashpublications.org
Up to 60% of cases of the autosomal recessive immunodeficiency hemophagocytic
lymphohistiocytosis (HLH) are associated with mutations in the perforin (PRF1) gene. In this …
lymphohistiocytosis (HLH) are associated with mutations in the perforin (PRF1) gene. In this …
[HTML][HTML] A functional analysis of the putative polymorphisms A91V and N252S and 22 missense perforin mutations associated with familial hemophagocytic …
I Voskoboinik, MC Thia, JA Trapani - Blood, 2005 - Elsevier
Up to 60% of cases of the autosomal recessive immunodeficiency hemophagocytic
lymphohistiocytosis (HLH) are associated with mutations in the perforin (PRF1) gene. In this …
lymphohistiocytosis (HLH) are associated with mutations in the perforin (PRF1) gene. In this …
A functional analysis of the putative polymorphisms A91V and N252S and 22 missense perforin mutations associated with familial hemophagocytic …
I Voskoboinik, MC Thia, JA Trapani - Blood, 2005 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: p> Up to 60% of cases of the autosomal recessive
immunodeficiency hemophagocytic lymphohistiocytosis (HLH) are associated with …
immunodeficiency hemophagocytic lymphohistiocytosis (HLH) are associated with …
[引用][C] A functional analysis of the putative polymorphisms A91V and N252S and 22 missense perforin mutations associated with familial hemophagocytic …
I VOSKOBOINIK, MC THIA, JA TRAPANI - Blood, 2005 - pascal-francis.inist.fr
A functional analysis of the putative polymorphisms A91V and N252S and 22 missense
perforin mutations associated with familial hemophagocytic lymphohistiocytosis CNRS Inist …
perforin mutations associated with familial hemophagocytic lymphohistiocytosis CNRS Inist …
A functional analysis of the putative polymorphisms A91V and N252S and 22 missense perforin mutations associated with familial hemophagocytic …
I Voskoboinik, MC Thia, JA Trapani - Blood, 2005 - europepmc.org
Up to 60% of cases of the autosomal recessive immunodeficiency hemophagocytic
lymphohistiocytosis (HLH) are associated with mutations in the perforin (PRF1) gene. In this …
lymphohistiocytosis (HLH) are associated with mutations in the perforin (PRF1) gene. In this …
A functional analysis of the putative polymorphisms A91V and N252S and 22 missense perforin mutations associated with familial hemophagocytic …
I Voskoboinik, MC Thia, JA Trapani - Blood, 2005 - pubmed.ncbi.nlm.nih.gov
Up to 60% of cases of the autosomal recessive immunodeficiency hemophagocytic
lymphohistiocytosis (HLH) are associated with mutations in the perforin (PRF1) gene. In this …
lymphohistiocytosis (HLH) are associated with mutations in the perforin (PRF1) gene. In this …