TY - JOUR T1 - Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesity JF - Orphanet journal of rare diseases Y1 - 2018 A1 - Liu, Katherine Y A1 - Sengillo, Jesse D A1 - Velez, Gabriel A1 - Jauregui, Ruben A1 - Sakai, Lynn Y A1 - Maumenee, Irene H A1 - Bassuk, Alexander G A1 - Mahajan, Vinit B A1 - Tsang, Stephen H VL - 13 ER -