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Article

Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II.

The New England journal of medicine - 19 Dec 1991

Gorevic P D, Munoz P C, Gorgone G, Purcell J J, Rodrigues M, Ghiso J, Levy E, Haltia M, Frangione B

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Share to Amino Acid Sequence
Share to Amyloidosis
Share to Base Sequence
Share to Calcium-Binding Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Corneal Dystrophies, Hereditary

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Identifiers

PMID: 1658654
DOI: 10.1056/NEJM199112193252505

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II.PMID 1658654Read ↗

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