Variable phenotypes of gyrate atrophy in siblings with a nonsense mutation in OAT gene.Published in:Ophthalmic Genetics, 2021, v. 42, n. 3, p. 300, doi. 10.1080/13816810.2020.1870149By:Sen, Sagnik;Kannan, Saraswathi Karuvel;Shanmugam, Ulaganathan;Rajan, Renu;Babu, Naresh;Vanniarajan, AyyasamyPublication type:Article