Screening for F508del as a first step in the molecular diagnosis of cystic fibrosis,

Míreanna Comhchosúla

• Prevalência da mutação ΔF508 no gene cystic fibrosis transmembrane conductance regulator em pacientes com fibrose cística em um centro de referência no Brasil Prevalence of ΔF508 mutation in the cystic fibrosis transmembrane conductance regulator gene among cystic fibrosis patients from a Brazilian referral center
  le: Andréia Marisa Bieger, et al.
  Foilsithe: (2012-12-01)
• Cystic fibrosis transmembrane conductance regulator mutations at a referral center for cystic fibrosis
  le: Coutinho, Cyntia Arivabeni de Araújo Correia, et al.
  Foilsithe: (2013)
• Polymorphisms in the glutathione pathway modulate cystic fibrosis severity: a cross-sectional study
  le: Marson, Fernando Augusto de Lima, et al.
  Foilsithe: (2014)
• Genetic interaction of GSH metabolic pathway genes in cystic fibrosis
  le: Marson, Fernando Augusto de Lima, et al.
  Foilsithe: (2013)
• Nasal Potential Difference in Cystic Fibrosis considering Severe CFTR Mutations
  le: Ng, Ronny Tah Yen, et al.
  Foilsithe: (2015)