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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).
- Source :
-
Amyloid . Sep2018, Vol. 25 Issue 3, p211-212. 2p. - Publication Year :
- 2018
- Subjects :
- *TRANSTHYRETIN
*AMYLOIDOSIS
*MUSCLE diseases
*NEUROPATHY
*CARDIOMYOPATHIES
Subjects
Details
- Language :
- English
- ISSN :
- 13506129
- Volume :
- 25
- Issue :
- 3
- Database :
- Academic Search Index
- Journal :
- Amyloid
- Publication Type :
- Academic Journal
- Accession number :
- 133291394
- Full Text :
- https://doi.org/10.1080/13506129.2018.1491398