J Meretoja. Show Affiliations »
Abstract
Entities: Disease Gene Mutation
Mesh: See more » AdolescentAdultAge FactorsAgedAmyloidosis/diagnosisAmyloidosis/epidemiologyAmyloidosis/geneticsAmyloidosis/mortalityConsanguinityCorneal Dystrophies, Hereditary/geneticsFacial Paralysis/geneticsFemaleFinlandHeterozygoteHomozygoteHumansKidney Diseases/geneticsMaleMiddle AgedPedigreePrognosisSex FactorsSkin ManifestationsSyndrome
Year: 1973 PMID: 4543600 DOI: 10.1111/j.1399-0004.1973.tb01140.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438