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Molecular Vision|February 5, 2019
Identification and functional analysis of a novel oculocerebrorenal syndrome of Lowe (<i>OCRL</i>) gene variant in two pedigrees with varying phenotypes including isolated congenital cataractAhmed K Shalaby, Peter Emery-Billcliff, Diana Baralle, et al.
Genes|December 30, 2025
Expanding the Genetic Spectrum in <i>IMPG1</i> and <i>IMPG2</i> RetinopathySaoud Al-Khuzaei, Ahmed K Shalaby, Jing Yu, et al.
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