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Chinese familial transthyretin amyloidosis with vitreous involvement is associated with the transthyretin mutation Gly83Arg: a case report and literature review

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Description of transthyretin S50A, S52P and G47A mutations in familial amyloidosis polyneuropathy

By González-Duarte Alejandra   Lem-Carrillo Mónica   Cárdenas-Soto Karla  

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Isolated heart transplantation for familial transthyretin (TTR) V122I cardiac amyloidosis

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A novel type of familial transthyretin amyloidosis, ATTR Asn124Ser, with co-localization of κ light chains

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