Ku C

References (1)

Title : Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome - Igelman_2021_Ophthalmic.Genet_42_664

Author(s) : Igelman AD , Ku C , da Palma MM , Georgiou M , Schiff ER , Lam BL , Sankila EM , Ahn J , Pyers L , Vincent A , Ferraz Sallum JM , Zein WM , Oh JK , Maldonado RS , Ryu J , Tsang SH , Gorin MB , Webster AR , Michaelides M , Yang P , Pennesi ME

Ref : Ophthalmic Genet , 42 :664 , 2021

Abstract :

PubMedSearch : Igelman_2021_Ophthalmic.Genet_42_664

PubMedID: 34223797

Gene_locus related to this paper: human-ABHD12

Ku C

References (1)

1. Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome - Igelman_2021_Ophthalmic.Genet_42_664