Unusual presentation of rare Phe33Leu mutation hereditary TTR cardiac amyloidosis.
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DOI: 10.2217/fca-2021-0130
Abstract: Introduction: Hereditary TTR cardiac amyloidosis (ATTRv-CM) is a progressive and rare autosomal dominant disease, causing the formation of insoluble amyloid fibrils that deposit in the heart and nervous tissue. Case description: The authors present a… read more here.
Keywords: hereditary ttr; cardiac amyloidosis; ttr cardiac; phe33leu mutation ... See more keywords