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Article

Characterization of Ancestral Origin of Cystic Fibrosis of Patients with New Reported Mutations in CFTR.

BioMed research international - 1 Jan 2020

Paz-Y-Miño César, Zambrano Ana Karina, Ruiz-Cabezas Juan Carlos, Armendáriz-Castillo Isaac, García-Cárdenas Jennyfer M, Guerrero Santiago, López-Cortés Andrés, Pérez-Villa Andy, Guevara-Ramírez Patricia, Yumiceba Verónica, Leone Paola E

Abstract excerpt

The incidence of cystic fibrosis (CF) and the frequency of the variants reported for CFTR depend on the population; furthermore, CF symptomatology is characterized by obstructive lung disease and pancreatic insufficiency among other symptoms, which are reliant on the individual's genotype. The Ecuadorian population is a mixture of Native Americans, Europeans, and Africans. That population admixture could be the...

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Identifiers

PMID: 32596391
DOI: 10.1155/2020/9074760
PMCID: PMC7288203

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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