De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome.
Heinen, Stefan
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome. [electronic resource] - Human mutation Mar 2006 - 292-3 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1098-1004
10.1002/humu.9408 doi
Animals
Base Sequence
Chromosomes, Human, Pair 1
Cohort Studies
Complement Factor H--genetics
Erythrocytes--cytology
Gene Conversion
Hemolytic-Uremic Syndrome--genetics
Humans
Models, Genetic
Molecular Sequence Data
Multigene Family
Mutation
Sequence Homology, Nucleic Acid
Sheep
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome. [electronic resource] - Human mutation Mar 2006 - 292-3 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1098-1004
10.1002/humu.9408 doi
Animals
Base Sequence
Chromosomes, Human, Pair 1
Cohort Studies
Complement Factor H--genetics
Erythrocytes--cytology
Gene Conversion
Hemolytic-Uremic Syndrome--genetics
Humans
Models, Genetic
Molecular Sequence Data
Multigene Family
Mutation
Sequence Homology, Nucleic Acid
Sheep