Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease (Q57232815)
Jump to navigation
Jump to search
scientific article published on 01 July 1992
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease |
scientific article published on 01 July 1992 |
Statements
Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease (English)
A de la Chapelle
C P Maury