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Article

Genetic microheterogeneity of human transthyretin detected by IEF.

Electrophoresis - 1 Jun 2007

Altland Klaus, Benson Merrill D, Costello Catherine E, Ferlini Alessandra, Hazenberg Bouke P C, Hund Ernst, Kristen Arnt V, Linke Reinhold P, Merlini Giampaolo, Salvi Fabrizio, Saraiva Maria J, Singer Reinhard, Skinner Martha, Winter Pia

Abstract excerpt

Mutations of the human transthyretin (TTR) gene have attracted medical interest as a cause of amyloidosis. Recently, we have described in detail an electrophoretic procedure with PAGE followed by IEF in urea gradients for the study of the microheterogeneity of TTR monomers (Altland, K., Winter, P., Sauerborn, M. K., Electrophoresis 1999, 20, 1349-1364). In this paper, we present a study on 49 different mutations...

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Identifiers

PMID: 17503405
DOI: 10.1002/elps.200600840

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TTR

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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