A COMPREHENSIVE AND VERSION-CONTROLLED DATABASE OF GLACIAL LAKE OUTBURST FLOODS IN HIGH MOUNTAIN ASIA





Clinical differential factors in patients with hereditary transthyretin amyloidosis with Val142Ile and Ser43Asn mutations

Abstract Background Hereditary transthyretin amyloidosis (hATTR) is a rare autosomal dominant disease with high clinical variability, influenced by both genotype and the geographic origins of carriers.There is a limited understanding of the Val142Ile and Ser43Asn recognised mutations in Ecuador and Colombia.Therefore, the objective of this study is

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