Human diseases that
include dyskeratosis congenita, aplastic anemia, and
idiopathic pulmonary fibrosis have been genetically linked to mutations that negatively affect telomerase activity and / or accelerate the loss of telomere length.
April 17, 2013 Gene study helps understand
pulmonary fibrosis A new study looking at the genomes of more than 1,500 patients with
idiopathic pulmonary fibrosis, a rare and devastating lung disease, found multiple genetic associations with the disease,
including one gene variant that was linked to an increase in the risk of death.