https://www.selleckchem.com/pr....oducts/selnoflast.ht
The phenotype of mutations at codon 289 of EDA in NSTA affected patients was characterized by lateral incisors loss, rarely affecting the maxillary first molars. A novel EDAR missense variant c.338GA (p.(Cys113Tyr)) was identified in a family with NSTA, extending the mutation spectrum of the EDAR gene. Genotype-phenotype correlation analyses of EDAR and EDA mutations could help to improve disease status prediction in NSTA families. A (p.(Cys113Tyr)) was identified in a family with NSTA, extending the mutation spectrum of the EDAR
Like
Comment
Share
