Genomic Screening Identifies Individuals at High Risk for Hereditary Transthyretin Amyloidosis

The TTR V142I variant associated with hereditary transthyretin amyloidosis (hATTR) is present in up to 4% of African American (AA) and 1% of Hispanic/Latinx (HL) individuals and increases risk for heart failure. Delayed and missed diagnoses could potentiate health disparities in these populations. W...

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Detalles Bibliográficos
Autores principales: Soper, Emily R., Suckiel, Sabrina A., Braganza, Giovanna T., Kontorovich, Amy R., Kenny, Eimear E., Abul-Husn, Noura S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829706/
https://www.ncbi.nlm.nih.gov/pubmed/33467513
http://dx.doi.org/10.3390/jpm11010049

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829706/
https://www.ncbi.nlm.nih.gov/pubmed/33467513
http://dx.doi.org/10.3390/jpm11010049

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