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Special article
Follow-up regimens for carriers of hereditary transthyretin variants
Seguimiento de portadores asintomáticos de variantes hereditarias de la transtirretina
Inés Asunción Losada-Lópeza,
Corresponding author
ialosada@hsll.es

Corresponding author.
, Solange Kapetanovic-Garcíab, Teresa Sevilla-Mantecónc, Francisco Muñoz-Beamudd
a Internal Medicine Service, Hospital Universitario Son Llátzer, Palma, Spain; Balearic Research Group in Genetic Cardiopathies, Sudden Death and TTR Amyloidosis, Instituto de Investigación Sanitaria de las Islas Baleares (IdISBa), Palma, Spain
b Unidad de ELA y neuromuscular, Hospital Universitario Basurto, Bilbao, Spain
c Hospital Universitari i Politècnic La Fe & IIS La Fe, Neuromuscular Diseases Unit, Department of Neurology, Valencia, Spain; Universitat de València, Valencia, Spain; Biomedical Research Network Center in Rare Diseases (CIBERER); Member of the European Reference Network for Rare Neuromuscular Diseases (ERN EURO-NMD), Spain
d Facultativo Especialista de Área de Medicina Interna, Unidad de Enfermedades Autoinmunes, Minoritarias y Trombosis, Coordinador Unidad Multidisciplinar de Amiloidosis Hereditaria, Servicio de Medicina Interna, Hospital Juan Ramón Jiménez, Spain
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ISSN: 00257753
Original language: English
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2023 March 16 10 26

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