Amyloidosis due to TTR mutations in Mexico with 4 distincts genotypes in the index cases-Reference-Cited by-同舟云学术

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Amyloidosis due to TTR mutations in Mexico with 4 distincts genotypes in the index cases

Published:2018-07-03 Issue:1 Volume:13 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

González-Duarte Alejandra,Cárdenas-Soto Karla,Bañuelos Carlo Enrico,Fueyo Omar,Dominguez Carolina,Torres Benjamín,Cantú-Brito Carlos

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-018-0801-y.pdf

Reference34 articles.

1. Planté-Bordeneuve V, Said G. Familial amyloid polyneuropathy. Lancet Neurol. 2011;10(2):1086–97.

2. Sousa A, Coelho T, Barros J et al. Genetic epidemiology of familial amylodotic polyneuropathy (FAP) type I in Povoa do Varzim and Vila do Conde (North of Portugal). Am J Med Genet 1995;60:512-521.

3. Coelho T, Ericzon B, Roy Grogan D. A Physician’s guide to Transthyretin Amyloidosis. Amyloidosis Fundation. 2010.

4. Rapezzi C, Riva L, Quarta C, et al. Gender-related risk of myocardial involvement in systemic amyloidosis. Amyloid. 2008;15(1):40–8.

5. Munar-Qués M, MasJuan J, Coelho T, et al. Familial amyloid polyneuropathy associated with TTRSer50Arg mutation in two Iberian families presenting a novel single base change in the mutant gene. Amyloid. 2007;14(2):147–52.

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