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Hereditary Transthyretin Amyloidosis in Eight Chinese Families
BACKGROUND: Mutations of transthyretin (TTR) cause the most common type of autosomal-dominant hereditary systemic amyloidosis, which occurs worldwide. To date, more and more mutations in the TTR gene have been reported. Some variations in the clinical presentation are often observed in patients with...
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| Publicado en: | Chin Med J (Engl) |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4756886/ https://ncbi.nlm.nih.gov/pubmed/26521788 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0366-6999.168048 |
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