IFNL3 Genetic Variant Linked to PF, but not to Skin Fibrosis in Patients with Systemic Sclerosis, Study Finds
A genetic variant at the IFNL3 gene is linked to raised levels of IFN-lambda 3 in the blood and is associated with the presence of pulmonary fibrosis in patients with systemic sclerosis, but it does not represent a risk factor for worsening of skin fibrosis in these patients, a…