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Ultra-rare C3 mutation leading to a dominant familial C3 glomerulopathy phenotype
Ultra-rare C3 mutation leading to a dominant familial C3 glomerulopathy phenotype
2017
Alexandria Leonhardt
Jill Hauer
Nicolo Ghiringhelli
Yuzhou Zhang
Nicole Meyer
Renee X. Goodfellow
Bertha Martin
Carla M. Nester
Richard Smith
Keywords:
Genetics
Molecular biology
Phenotype
Glomerulopathy
Mutation
Biology
Correction
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