Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry

IMPORTANCE: Hereditary transthyretin (TTR) amyloid cardiomyopathy (hATTR-CM) due to the TTR V122I variant is an autosomal-dominant disorder that causes heart failure in elderly individuals of African ancestry. The clinical associations of carrying the variant, its effect in other African ancestry po...

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Detalles Bibliográficos
Publicado en:JAMA
Main Authors: Damrauer, Scott M., Chaudhary, Kumardeep, Cho, Judy H., Liang, Lusha W., Argulian, Edgar, Chan, Lili, Dobbyn, Amanda, Guerraty, Marie A., Judy, Renae, Kay, Jenna, Kember, Rachel L., Levin, Michael G., Saha, Aparna, Van Vleck, Tielman, Verma, Shefali S., Weaver, JoEllen, Abul-Husn, Noura S., Baras, Aris, Chirinos, Julio A., Drachman, Brian, Kenny, Eimear E., Loos, Ruth J. F., Narula, Jagat, Overton, John, Reid, Jeffrey, Ritchie, Marylyn, Sirugo, Giorgio, Nadkarni, Girish, Rader, Daniel J., Do, Ron
Formato: Artigo
Idioma:Inglês
Publicado: American Medical Association 2019
Assuntos:
Original Investigation
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7081752/
https://ncbi.nlm.nih.gov/pubmed/31821430
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jama.2019.17935
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