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Hereditary Transthyretin Amyloidosis: Case Studies

Over 130 genetic mutations have been described that contribute to hereditary TTR amyloidosis. This interactive, case-based webinar explains the pathogenesis, genetics, and manifestations of this disease and offers counseling recommendations and resources. Discussions between expert physicians and specialized genetic counselors bring patient cases to life in this interactive activity. Resources for genetic counselors and their patients are also available.
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