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

Authors :
Patel, Kavisha
Tagoe, Clement
Bieri, Phyllis
Weidenheim, Karen
Tauras, James M.
Source :
Amyloid; Sep2018, Vol. 25 Issue 3, p211-212, 2p
Publication Year :
2018

Subjects

Subjects :
TRANSTHYRETIN
AMYLOIDOSIS
MUSCLE diseases
NEUROPATHY
CARDIOMYOPATHIES

Details

Language :
English
ISSN :
13506129
Volume :
25
Issue :
3
Database :
Complementary Index
Journal :
Amyloid
Publication Type :
Academic Journal
Accession number :
133291394
Full Text :
https://doi.org/10.1080/13506129.2018.1491398
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