Phenotypic Characterization of the c.1679+1643G>T (1811+1643G>T) Mutation in Hispanic Cystic Fibrosis Patients

Author:

Fanous HaniORCID,Delgado-Villata Silvia,Kovacs Reka,Shalaby-Rana Eglal,Sami-Zakahri Iman

Publisher

MDPI AG

Subject

General Medicine

Reference13 articles.

1. 2014 Annual Data Report;Registry,2015

2. Cystic fibrosis

3. Disease modifying genes in cystic fibrosis

4. Comparison of the clinical manifestations of cystic fibrosis in black and white patients

5. A novel donor splice site in intron 11 of the CFTR gene, created by mutation 1811+1.6kbA>G, produces a new exon: High frequency in spanish cystic fibrosis chromosomes and association with severe phenotype;Chillon;Am. J. Hum. Genet.,1995

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