Ocular Manifestations of Alport Syndrome: Report and Comparison of Two Cases

por Sargazi, Meisam, Dehghani, Shima, Dahmardeh, Mina, Mohammadi, Seyed Omid
Publicado 2023

Hypotrichosis with juvenile macular dystrophy: Combination of whole‐genome sequencing and genome‐wide homozygosity mapping identifies a large deletion in CDH3 initially undetected...

por Saeidian, Amir Hossein, Vahidnezhad, Hassan, Youssefian, Leila, Sotudeh, Soheila, Sargazi, Meisam, Zeinali, Sirous, Uitto, Jouni
Publicado 2019