Multiple Vitelliform Lesions as a Retinal Manifestation of Alport Syndrome

por Eriksen, Kathrine O., Jørstad, Øystein Kalsnes
Publicado 2020

A novel homozygous variant in the SPG7 gene presenting with childhood optic nerve atrophy

por Eriksen, Kathrine O., Wigers, Andreas Reidar, Wedding, Iselin Marie, Erichsen, Anne Kjersti, Barøy, Tuva, Søberg, Kristoffer, Jørstad, Øystein Kalsnes
Publicado 2022