Analysis of cystic fibrosis gene mutations in children with cystic fibrosis and in 964 infertile couples within the region of Basilicata, Italy: a research study

INTRODUCTION: Cystic fibrosis is the most common autosomal recessive genetic disease in the Caucasian population. Extending knowledge about the molecular pathology on the one hand allows better delineation of the mutations in the CFTR gene and the other to dramatically increase the predictive power...

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Detalles Bibliográficos
Autores principales: Dell’Edera, Domenico, Benedetto, Michele, Gadaleta, Gemma, Carone, Domenico, Salvatore, Donatello, Angione, Antonella, Gallo, Massimiliano, Milo, Michele, Pisaturo, Maria Laura, Di Pierro, Giuseppe, Mazzone, Eleonora, Epifania, Annunziata Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196456/
https://www.ncbi.nlm.nih.gov/pubmed/25304080
http://dx.doi.org/10.1186/1752-1947-8-339

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196456/
https://www.ncbi.nlm.nih.gov/pubmed/25304080
http://dx.doi.org/10.1186/1752-1947-8-339

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