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Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease.
- Source :
-
Genomics [Genomics] 1992 Jul; Vol. 13 (3), pp. 902-3. - Publication Year :
- 1992
Details
- Language :
- English
- ISSN :
- 0888-7543
- Volume :
- 13
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Genomics
- Publication Type :
- Academic Journal
- Accession number :
- 1322360
- Full Text :
- https://doi.org/10.1016/0888-7543(92)90183-s