Login / Signup

Interaction among variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1, and SLC9A3) and CFTR mutations with clinical markers of cystic fibrosis.

Stephanie V N PereiraJose D RibeiroCarmen S BertuzzoFernando Augusto Lima Marson
Published in: Pediatric pulmonology (2018)
Interaction between variants in the SLC family genes and the grouping for CFTR mutations were associated with PI, onset of digestive symptoms and mucoid P. aeruginosa, being important to determine one of the factors that may cause the diversity among the patients with CF.
Keyphrases
  • cystic fibrosis
  • pseudomonas aeruginosa
  • copy number
  • lung function
  • genome wide
  • depressive symptoms
  • chronic obstructive pulmonary disease
  • genome wide analysis