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Determination of Cystic Fibrosis Mutation Frequency in Preterm and Term Neonates with Respiratory Tract Problems

Cystic fibrosis (CF) is an autosomal recessive disease. The genetic transition occurs with CF transmembrane conductance regulator (CFTR) gene mutation. We aimed to determine the frequency of CF mutations and also new mutations in the CFTR gene in neonates with respiratory distress. Newborn babies ho...

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Detalles Bibliográficos
Autores principales: Tanriverdi, S, Polat, M, Onay, H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524182/
https://www.ncbi.nlm.nih.gov/pubmed/36249513
http://dx.doi.org/10.2478/bjmg-2021-0023