Novel compound heterozygous mutations in the C3 gene: hereditary C3 deficiency

Subjects

Subjects :

Male
Heterozygote
Codon, Nonsense
Child, Preschool
Mutation
Humans
Complement C3
Exons
RNA Splice Sites
Sequence Analysis, DNA
Metabolism, Inborn Errors

Details

ISSN :

1442200X

Volume :

53

Issue :

2

Database :

OpenAIRE

Journal :

Pediatrics international : official journal of the Japan Pediatric Society

Accession number :

edsair.pmid..........2f26a70adb3f0b711db79d2c57d47c1c