A Patient With Hereditary ATTR and a Novel AGel p.Ala578Pro Amyloidosis

Hereditary amyloidosis represents a group of diseases in which mutant proteins are deposited in various organs leading to their dysfunction. Correct identification of the amyloid-causing protein is critical because this will determine the optimal therapy for the patient. The most common type of here...

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Veröffentlicht in:Mayo Clinic proceedings 2018-11, Vol.93 (11), p.1678-1682
Hauptverfasser: Sridharan, Meera, Highsmith, W. Edward, Kurtin, Paul J., Zimmermann, Michael T., Theis, Jason D., Dasari, Surendra, Dingli, David
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Sprache:eng
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