Login / Signup

Filamin A gene mutation in an infant with progressive pulmonary emphysema, periventricular nodular heterotopia and congenital heart disease.

Sanjeev KheraShilpa JauhariSomali PattanayakMrigank Choubey
Published in: BMJ case reports (2024)
Keyphrases
  • congenital heart disease
  • pulmonary hypertension
  • multiple sclerosis
  • chronic obstructive pulmonary disease
  • lung function
  • pulmonary fibrosis
  • idiopathic pulmonary fibrosis
  • cystic fibrosis
  • air pollution