Kamron N. Khan

Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

Gavin Arno, Smriti A. Agrawal, Aiden Eblimit et al. · The American Journal of Human Genetics · 2016 · 129 citations · Full text

Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects

Kamron N. Khan, Clare V. Logan, Martin McKibbin et al. · Human Molecular Genetics · 2011 · 94 citations · Full text

Ocular Disease, Genetics, Molecular Genetics +20

Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma

Kamron N. Khan, Adam K Rudkin, David Parry et al. · The American Journal of Human Genetics · 2011 · 79 citations · Full text

Homozygous Mutations, Congenital Cataract-microcornea, Ocular Disease +13

Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy

Kamron N. Khan, Melissa Kasilian, Omar A. Mahroo et al. · Ophthalmology · 2018 · 79 citations · Full text

Clinical and Genetic Features of Choroideremia in Childhood

Kamron N. Khan, Farrah Islam, Anthony T. Moore et al. · Ophthalmology · 2016 · 78 citations

Inherited Metabolic Disease, Pediatrics, Choroid Plexus +4