De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

S Heinen, P Sanchez‐Corral, MS Jackson… - Human …, 2006 - Wiley Online Library
Many of the complement regulatory genes within the RCA cluster (1q32) have arisen
through genomic duplication and the resulting high degree of sequence identity is likely to …

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

S Heinen, P Sanchez-Corral, MS Jackson… - Human …, 2006 - pubmed.ncbi.nlm.nih.gov
Many of the complement regulatory genes within the RCA cluster (1q32) have arisen
through genomic duplication and the resulting high degree of sequence identity is likely to …

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

S Heinen, P Sanchez-Corral, MS Jackson… - Human …, 2006 - eprints.ncl.ac.uk
Many of the complement regulatory genes within the RCA cluster (1q32) have arisen
through genomic duplication and the resulting high degree of sequence identity is likely to …

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

S Heinen, P Sanchez-Corral, MS Jackson… - Human …, 2006 - search.proquest.com
Many of the complement regulatory genes within the RCA cluster (1q32) have arisen
through genomic duplication and the resulting high degree of sequence identity is likely to …

[PDF][PDF] De Novo Gene Conversion in the RCA Gene Cluster (1q32) Causes Mutations in Complement Factor H Associated With Atypical Hemolytic Uremic Syndrome

S Heinen, P Sanchez-Corral, MS Jackson, L Strain… - 2006 - academia.edu
The RCA (Regulators of Complement Activation) gene cluster on human chromosome 1q32
spans a total of 21.45 cM and contains more than 60 genes of which 15 are complement …

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome.

S Heinen, P Sanchez-Corral, MS Jackson, L Strain… - Human …, 2006 - europepmc.org
Many of the complement regulatory genes within the RCA cluster (1q32) have arisen
through genomic duplication and the resulting high degree of sequence identity is likely to …

[PDF][PDF] De Novo Gene Conversion in the RCA Gene Cluster (1q32) Causes Mutations in Complement Factor H Associated With Atypical Hemolytic Uremic Syndrome

S Heinen, P Sanchez-Corral, MS Jackson, L Strain… - 2006 - Citeseer
The RCA (Regulators of Complement Activation) gene cluster on human chromosome 1q32
spans a total of 21.45 cM and contains more than 60 genes of which 15 are complement …

[引用][C] De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

S Heinen, P Sanchez-Corral, MS Jackson, L Strain… - Human Mutation, 2006 - cir.nii.ac.jp
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement
factor H associated with atypical hemolytic uremic syndrome | CiNii Research CiNii 国立情報学 …

[引用][C] De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

S Heinen, P Sanchez-Corral, MS Jackson… - Human …, 2006 - researchportal.helsinki.fi
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement
factor H associated with atypical hemolytic uremic syndrome — University of Helsinki Skip to …

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

S Heinen, P Sánchez-Corral, M Jackson, L Strain… - 2006 - digital.csic.es
Many of the complement regulatory genes within the RCA cluster (1q32) have arisen
through genomic duplication and the resulting high degree of sequence identity is likely to …