DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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References
Hiltunen T, Kiuru S, Hongell V. et al.
Finnish type of familial amyloidosis: cosegregation of ASP187→ASN mutation of gelsolin with the disease in three large families.
Am J Hum Genet 1991;
49: 522-528
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