AHI1 gene mutation in a consanguineous Iranian family affected by Joubert syndrome: A case report

por Neissi, Mostafa, Mabudi, Hadideh, Mohammadi‐Asl, Javad
Publicado 2021

Identification of a Novel WFS1 Mutation Using the Whole Exome Sequencing in an Iranian Pedigree with Autosomal Dominant Hearing Loss

por Mohammadi-asl, Javad, Saki, Nader, Dehdashtiyan, Masoud, Neissi, Mostafa, Ghanbari Mardasi, Farideh
Publicado 2021