De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome-Reference-Cited by-同舟云学术

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

Published:2006-03 Issue:3 Volume:27 Page:292-293
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Heinen Stefan,Sanchez-Corral Pilar,Jackson Michael S,Strain Lisa,Goodship Judith A.,Kemp Elizabeth J.,Skerka Christine,Jokiranta T. Sakari,Meyers Kevin,Wagner Eric,Robitaille Pierre,Esparza-Gordillo Jorge,Rodriguez de Cordoba Santiago,Zipfel Peter F.,Goodship Timothy H.J.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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4. The absence of CFHR3 and CFHR1 genes from the T2T-CHM13 assembly can limit the molecular diagnosis of complement-related diseases;European Journal of Human Genetics;2023-04-10

5. An ex vivo test to investigate genetic factors conferring susceptibility to atypical haemolytic uremic syndrome;Frontiers in Immunology;2023-02-09

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