Reporting Two Novel Mutations in Two Iranian Families with Cystic Fibrosis, Molecular and Bioinformatic Analysis

BACKGROUND: Cystic fibrosis is the most common heredity disease among the Caucasian population. More than 350 known pathogenic variations in the CFTR gene (NM_000492.4) cause CF. Herein, we report the outcome of our investigation in two unrelated Iranian families with CF patients. METHODS: We conduc...

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Detalles Bibliográficos
Autores principales: Hosseini Nami, Amin, Kabiri, Mahboubeh, Zeinali, Sirous
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pasteur Institute of Iran 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763878/
https://www.ncbi.nlm.nih.gov/pubmed/35468710
http://dx.doi.org/10.52547/ibj.3713

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763878/
https://www.ncbi.nlm.nih.gov/pubmed/35468710
http://dx.doi.org/10.52547/ibj.3713

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