S-EPMC11969550 - A novel heterozygous mutation in the gelsolin gene causes Finnish gelsolin amyloidosis associated with nephropathy and thrombotic microangiopathy. - OmicsDI

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A novel heterozygous mutation in the gelsolin gene causes Finnish gelsolin amyloidosis associated with nephropathy and thrombotic microangiopathy.

ABSTRACT:

SUBMITTER: Liang H

PROVIDER: S-EPMC11969550 | biostudies-literature | 2025

REPOSITORIES: biostudies-literature