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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Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: American Medical Association 2019
Fag:
Original Investigation
Online adgang: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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