Characterization of a large genomic deletion in four Irish families with C7 deficiency
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Immunology
Reference16 articles.
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4. Hereditary deficiency of the seventh component of complement and recurrent meningococcal infection: investigations of an Irish family using a novel haemolytic screening assay for complement activity and C7 M/N allotyping;Egan;Epidemiol. Infect.,1994
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1. Genetic bases of C7 deficiency: systematic review and report of a novel deletion determining functional hemizygosity;Frontiers in Immunology;2023-05-25
2. Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese;National Science Review;2018-11-05
3. C7;The Complement FactsBook;2018
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