Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease (Q57232815)
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scientific article published on 01 July 1992
Language | Label | Description | Also known as |
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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