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Amyloidosis due to TTR mutations in Mexico with 4 distincts genotypes in the index cases
BACKGROUND: Transthyretin-related hereditary amyloidosis (ATTR) is a systemic disease characterized by extracellular deposits of amyloid due to the autosomal dominant inheritance of a mutation in the TTR gene (18q12.1). Although described worldwide, it is a rare disease, limited to certain parts of...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029070/ https://www.ncbi.nlm.nih.gov/pubmed/29970125 http://dx.doi.org/10.1186/s13023-018-0801-y |