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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 Maury  1 , J Kere, R Tolvanen, A de la Chapelle
Affiliations
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.
No abstract available

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