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Deep Phenotyping of F64L Mutation in a Multicentric Cohort of Patisiran-Treated Hereditary Transthyretin Amyloidosis Patients (Patisiranitaly)

Ceccanti M et al.
Europe PMC · Papers · License: Open Access
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Transthyretin Amyloidosis, Nt‐probnp, Attrv, F64l Mutation, P. Phe84leu
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Record · ID 266531
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