Tyr78Phe Transthyretin Mutation with Predominant Motor Neuropathy as the Initial Presentation
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Transthyretin (TTR) amyloidosis, the most frequent form of hereditary amyloidosis, is caused by dominant mutations in the TTR gene. More than 100 mutations have been identified. Clinical manifestations of TTR amyloidosis are usually induced by extracellular am... ...
