@article{aeaab7de333a4d12be521a993d540e88,
title = "Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study",
keywords = "Gelsolin, Amyloidosis, AGel, Hereditary amyloidosis, Meretoja syndrome, Natural history, Lifespan, Relative survival, LATTICE CORNEAL-DYSTROPHY, FAMILIAL AMYLOIDOSIS, RENAL AMYLOIDOSIS, NEPHROTIC SYNDROME, MUTATION, VARIANT, POLYNEUROPATHY, POPULATION, GENE, FAF, 1184 Genetics, developmental biology, physiology",
author = "Eeva-Kaisa Schmidt and Tuuli Mustonen and Sari Kiuru-Enari and Kivel{\"a}, {Tero T.} and Sari Atula",
year = "2020",
month = jan,
day = "17",
doi = "10.1186/s13023-020-1300-5",
language = "English",
volume = "15",
journal = "Orphanet journal of rare diseases",
issn = "1750-1172",
publisher = "BMC",
number = "1",
}