The Functional Basis for Hemophagocytic Lymphohistiocytosis in a Patient with Co-inherited Missense Mutations in the Perforin (PFN1) Gene

I Voskoboinik, MC Thia, A De Bono, K Browne… - The Journal of …, 2004 - rupress.org
About 30% of cases of the autosomal recessive immunodeficiency disorder hemophagocytic
lymphohistiocytosis are believed to be caused by inactivating mutations of the perforin gene …
被引用次数：89 相关文章

The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited missense mutations in the perforin (PFN1) gene.

I Voskoboinik, MC Thia, A De Bono… - The Journal of …, 2004 - europepmc.org
About 30% of cases of the autosomal recessive immunodeficiency disorder hemophagocytic
lymphohistiocytosis are believed to be caused by inactivating mutations of the perforin gene …
[PDF] academia.edu

[PDF][PDF] The Functional Basis for Hemophagocytic Lymphohistiocytosis in a Patient with Co-inherited Missense Mutations in the Perforin (PFN1) Gene

I Voskoboinik, MC Thia, A De Bono, K Browne… - academia.edu
About 30% of cases of the autosomal recessive immunodeficiency disorder hemophagocytic
lymphohistiocytosis are believed to be caused by inactivating mutations of the perforin gene …
[HTML] nih.gov

[HTML][HTML] The Functional Basis for Hemophagocytic Lymphohistiocytosis in a Patient with Co-inherited Missense Mutations in the Perforin (PFN1) Gene

I Voskoboinik, MC Thia, A De Bono… - The Journal of …, 2004 - ncbi.nlm.nih.gov
About 30% of cases of the autosomal recessive immunodeficiency disorder hemophagocytic
lymphohistiocytosis are believed to be caused by inactivating mutations of the perforin gene …
[PDF] researchgate.net

[PDF][PDF] The Functional Basis for Hemophagocytic Lymphohistiocytosis in a Patient with Co-inherited Missense Mutations in the Perforin (PFN1) Gene

I Voskoboinik, MC Thia, A De Bono, K Browne… - researchgate.net
About 30% of cases of the autosomal recessive immunodeficiency disorder hemophagocytic
lymphohistiocytosis are believed to be caused by inactivating mutations of the perforin gene …
[PDF] semanticscholar.org

[PDF][PDF] The Functional Basis for Hemophagocytic Lymphohistiocytosis in a Patient with Co-inherited Missense Mutations in the Perforin (PFN1) Gene

I Voskoboinik, MC Thia, A De Bono, K Browne… - pdfs.semanticscholar.org
About 30% of cases of the autosomal recessive immunodeficiency disorder hemophagocytic
lymphohistiocytosis are believed to be caused by inactivating mutations of the perforin gene …

The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited missense mutations in the perforin (PFN1) gene

I Voskoboinik, MC Thia, A De Bono… - The Journal of …, 2004 - pubmed.ncbi.nlm.nih.gov
About 30% of cases of the autosomal recessive immunodeficiency disorder hemophagocytic
lymphohistiocytosis are believed to be caused by inactivating mutations of the perforin gene …

[引用][C] The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited missense mutations in the perforin (PRF1) gene

I VOSKOBOINIK - J Exp Med., 2004 - cir.nii.ac.jp
The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited
missense mutations in the perforin (PRF1) gene | CiNii Research CiNii 国立情報学研究所 学術 …
[PDF] unimelb.edu.au

[PDF][PDF] The Functional Basis for Hemophagocytic Lymphohistiocytosis in a Patient with Co-inherited Missense Mutations in the Perforin (PFN1) Gene

I Voskoboinik, MC Thia, A De Bono, K Browne… - minerva-access.unimelb.edu.au
About 30% of cases of the autosomal recessive immunodeficiency disorder hemophagocytic
lymphohistiocytosis are believed to be caused by inactivating mutations of the perforin gene …
[PDF] psu.edu

[PDF][PDF] The Functional Basis for Hemophagocytic Lymphohistiocytosis in a Patient with Co-inherited Missense Mutations in the Perforin (PFN1) Gene

I Voskoboinik, MC Thia, A De Bono, K Browne… - Citeseer
About 30% of cases of the autosomal recessive immunodeficiency disorder hemophagocytic
lymphohistiocytosis are believed to be caused by inactivating mutations of the perforin gene …