Reappraisal of Frequency of Common Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations in Iranian Cystic Fibrosis Patients

BACKGROUND: Cystic Fibrosis (CF) is a life-threatening recessive genetic disorder resulting from mutations in the gene encoding the fibrosis transmembrane conductance regulator protein (CFTR). The CF clinical phenotype shows wide variation ranging from severe disease in early childhood in those homo...

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Detaylı Bibliyografya
Yayımlandı:Tanaffos
Asıl Yazarlar: Khalilzadeh, Soheila, Hassanzad, Maryam, PourAbdollah Toutkaboni, Mihan, Tashayoie Nejad, Sabereh, Sheikholeslami, Fatemeh-Maryam, Velayati, Ali Akbar
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Research Institute of Tuberculosis and Lung Disease 2018
Konular:
Original Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6320558/
https://ncbi.nlm.nih.gov/pubmed/30627177
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