Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Orphanet journal of rare diseases - 3 Jul 2018

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

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Aged
Share to Amyloidosis
Share to Genotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mexico

Share to Mutation

Share to Prealbumin

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 29970125
DOI: 10.1186/s13023-018-0801-y
PMCID: PMC6029070

Genes

TTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Amyloidosis due to TTR mutations in Mexico with 4 distincts genotypes in the index cases.PMID 29970125Read ↗

Transthyretin-related hereditary amyloidosis in an Argentinian family with TTR Tyr114Cys mutation.Semantic proximity Read ↗

The genetic heterogeneity of hereditary transthyretin amyloidosis in a sample of the Brazilian population.Semantic proximity Read ↗

Genotype-Phenotype Correlations in ATTR Amyloidosis: A Clinical Update.Semantic proximity Read ↗

Clinical and genetic profiles of patients with hereditary and wild-type transthyretin amyloidosis: the Transthyretin Cardiac Amyloidosis Registry in the state of São Paulo, Brazil (REACT-SP)Semantic proximity Read ↗

Frequencies and geographic distributions of genetic mutations in transthyretin- and non-transthyretin-related familial amyloidosis.Semantic proximity Read ↗

Molecular mechanisms of amyloidosis.Semantic proximity Read ↗

Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis.Semantic proximity Read ↗

Epidemiology of variant transthyretin amyloidosis at a reference center in Argentina.Semantic proximity Read ↗

Experience of Hereditary Amyloidosis with Rare Variant in Ecuador: A Series of CasesSemantic proximity Read ↗

Online registry for mutations in hereditary amyloidosis including nomenclature recommendations.Semantic proximity Read ↗

Clinical and Phenotypic Characterization of Hereditary Transthyretin Amyloidosis (ATTRv) in Peruvian Population: First Case Series IMPAC-FE StudySemantic proximity Read ↗

A novel p.Gly417Valfs*12 mutation in the MTTP gene causing abetalipoproteinemia: Presentation of the first patient in Mexico and analysis of the previously reported cases.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.