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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Publicado en:JAMA
Autores principales: 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
Lenguaje:Inglês
Publicado: American Medical Association 2019
Materias:
Original Investigation
Acceso en línea: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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