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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. 25:211-212
- Publication Year :
- 2018
- Publisher :
- Informa UK Limited, 2018.
- Subjects :
- 0301 basic medicine
Pathology
medicine.medical_specialty
biology
business.industry
Amyloidosis
Cardiomyopathy
medicine.disease
03 medical and health sciences
Amyloid Neuropathy
Transthyretin
030104 developmental biology
0302 clinical medicine
Mutation (genetic algorithm)
Internal Medicine
biology.protein
Medicine
medicine.symptom
business
Myopathy
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 17442818 and 13506129
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- Amyloid
- Accession number :
- edsair.doi...........af42655d006ae592139bd26f31ad25d5
- Full Text :
- https://doi.org/10.1080/13506129.2018.1491398