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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Tanaffos
Päätekijät: Khalilzadeh, Soheila, Hassanzad, Maryam, PourAbdollah Toutkaboni, Mihan, Tashayoie Nejad, Sabereh, Sheikholeslami, Fatemeh-Maryam, Velayati, Ali Akbar
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: National Research Institute of Tuberculosis and Lung Disease 2018
Aiheet:
Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6320558/
https://ncbi.nlm.nih.gov/pubmed/30627177
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia