https://gdc-0994inhibitor.com/....risk-factors-regardi
Transthyretin (TTR) gene mutations will be the typical cause of genetic amyloidosis. Valine replaced by isoleucine in position 122 (V122I) variant is common, particularly in the black populace. Providers of V122I have increased threat for establishing cardiac amyloidosis. Despite a relatively high prevalence, the penetrance of V122I is certainly not securely founded. This research sought to look for the prevalence of clinically evident cardiac amyloidosis amon
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