Life paths of patients with transthyretin-related familial amyloid polyneuropathy Val30Met: a descriptive study
Transthyretin-related familial amyloid polyneuropathy Val30Met is a fatal progressive disease. It is a rare hereditary amyloidosis, manifesting as a sensorimotor neuropathy and autonomic dysfunction. It begins during adulthood and is a disabling disease, posing a great psychological burden to patien...
| Autor principal: | |
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| Outros Autores: | , , , , , , |
| Formato: | article |
| Idioma: | eng |
| Publicado em: |
2018
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| Assuntos: | |
| Texto completo: | http://hdl.handle.net/10216/113023 |
| País: | Portugal |
| Oai: | oai:repositorio-aberto.up.pt:10216/113023 |