Associated Papers
A novel GSN variant outside the G2 calcium-binding domain associated with Amyloidosis of the Finnish type.
Mullany S et al.
Human Mutation, 2021
Cardiac conduction alterations in a French family with amyloidosis of the Finnish type with the p.Asp187Tyr mutation in the GSN gene.
Chastan N et al.
Muscle & Nerve, 2006
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