Karin W. Littink

Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa

Rob W.J. Collin, Karin W. Littink, B. Jeroen Klevering et al. · The American Journal of Human Genetics · 2008 · 164 citations · Full text

Ocular Disease, Developmental Biology, Retina +9

BBS1 Mutations in a Wide Spectrum of Phenotypes Ranging From Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome

Alejandro Estrada‐Cuzcano, Robert K. Koenekoop, Audrey Sénéćhal et al. · Archives of Ophthalmology · 2012 · 125 citations

Homozygosity Mapping in Patients with Cone–Rod Dystrophy: Novel Mutations and Clinical Characterizations

Karin W. Littink, Robert K. Koenekoop, L. Ingeborgh van den Born et al. · Investigative Ophthalmology & Visual Science · 2010 · 111 citations · Full text

Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa

Isabel Barragán, Salud Borrego, Juan I. Pieras et al. · Human Mutation · 2010 · 89 citations · Full text

Mutations in C2ORF71 Cause Autosomal-Recessive Retinitis Pigmentosa

Rob W.J. Collin, Christine Safieh, Karin W. Littink et al. · The American Journal of Human Genetics · 2010 · 87 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +4