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Case Reports

. 1992 Jul;13(3):902-3.

doi: 10.1016/0888-7543(92)90183-s.

Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease

C P Maury¹, J Kere, R Tolvanen, A de la Chapelle

Affiliations

PMID: 1322360
DOI: 10.1016/0888-7543(92)90183-s

Case Reports

Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease

C P Maury et al. Genomics. 1992 Jul.

. 1992 Jul;13(3):902-3.

doi: 10.1016/0888-7543(92)90183-s.

Authors

C P Maury¹, J Kere, R Tolvanen, A de la Chapelle

Affiliation

¹ Fourth Department of Medicine, University of Helsinki, Finland.

PMID: 1322360
DOI: 10.1016/0888-7543(92)90183-s

No abstract available

PubMed Disclaimer

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