K Berg, A Heiberg. Show Affiliations »
Abstract
Entities: Disease Mutation
Mesh: See more » Complement C3/geneticsGenetic LinkageHumansHypercholesterolemia/geneticsPolymorphism, GeneticRecombination, GeneticXanthomatosis/genetics
Substances: See more » Complement C3
Year: 1978 PMID: 752554 DOI: 10.1159/000131037
Source DB: PubMed Journal: Cytogenet Cell Genet ISSN: 0301-0171