Genotype study of filaggrin gene loss-of-function mutations in central India population with atopic dermatitis and ichthyosis vulgaris

• Auteurs principaux: Harsimran S Chawla (Auteur), Susmit Kosta (Auteur), Chaitanya Namdeo (Auteur), Rajesh Kataria (Auteur), Kailash Bhatia (Auteur), Roshni Sahu (Auteur), Pallavi Joshi (Auteur)
• Format: Livre
• Publié: Wolters Kluwer Medknow Publications, 2023-01-01T00:00:00Z.
• Sujets: article
• Accès en ligne: Connect to this object online.

Background: A genotype study of filaggrin gene loss-of-function mutations in central India can provide valuable insights into the prevalence and association of these mutations with atopic dermatitis (AD) and ichthyosis vulgaris (IV) in the region. The FLG R501X and 2282del4 are both genetic variants...