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...

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Detalles Bibliográficos
Autores principales: González-Duarte, Alejandra, Cárdenas-Soto, Karla, Bañuelos, Carlo Enrico, Fueyo, Omar, Dominguez, Carolina, Torres, Benjamín, Cantú-Brito, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
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

Internet

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

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