A case of transthyretin amyloidosis with myopathy, neuropathy, and cardiomyopathy resulting from an exceedingly rare mutation transthyretin Ala120Ser (c.418G > T, p.Ala140Ser)

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Bibliographic Details
Published in:Amyloid 2018-07, Vol.25 (3), p.211-212
Main Authors: Patel, Kavisha, Tagoe, Clement, Bieri, Phyllis, Weidenheim, Karen, Tauras, James M.
Format: Article
Language:English
Subjects:
Aged
Amyloid Neuropathies - genetics
Amyloid Neuropathies - pathology
Amyloid Neuropathies, Familial - genetics
Amyloid Neuropathies, Familial - pathology
Cardiomyopathies - genetics
Cardiomyopathies - pathology
Humans
Male
Mutation
Prealbumin - genetics
Prognosis
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ISSN:1350-6129
1744-2818
DOI:10.1080/13506129.2018.1491398