Association of TNF-α Gene Variants With Clinical Manifestation of Cystic Fibrosis Patients of Iranian Azeri Turkish Ethnicity

BACKGROUND: Cystic fibrosis (CF), a life-limiting autosomal recessive disorder, is considered a monogenic disease that is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. According to several studies, mutation analysis of the cystic fibrosis transmembrane c...

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Detalles Bibliográficos
Autores principales: Khorrami, Aziz, Bonyadi, Mortaza, Rafeey, Mandana, Omrani, Omid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505978/
https://www.ncbi.nlm.nih.gov/pubmed/26199696
http://dx.doi.org/10.5812/ijp.307

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505978/
https://www.ncbi.nlm.nih.gov/pubmed/26199696
http://dx.doi.org/10.5812/ijp.307

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