[The gene defect for Finnish hereditary amyloidosis has been found]
Duodecim
.
1991;107(16):1344-5.
[Article in Finnish]
Authors
C P Maury
,
J Kere
,
M Baumann
,
A de la Chapelle
PMID:
1365358
No abstract available
Publication types
Editorial
Review
MeSH terms
Amyloidosis / genetics*
Chromosome Aberrations
Chromosome Disorders
Finnland
Gelsolin / genetics*
Genes, Dominant
Humans
Mutation
Substances
Gelsolin