Collin, Rob W.J.

Non-syndromic retinitis pigmentosa

Verbakel, S. K., van Huet, R. A. C., Boon, C. J. F., den Hollander, A. I., Collin, R. W. J., Klaver, C. C. W., Hoyng, C. B., Roepman, R., & Klevering, B. J. (2018) · Progress in Retinal and Eye Research

Retinal Development and DisordersRetinal Diseases and Treatments

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Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations

Cremers, F. P. M., Lee, W., Collin, R. W. J., & Allikmets, R. (2020) · Progress in Retinal and Eye Research

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 315

Molecular Therapies for Inherited Retinal Diseases—Current Standing, Opportunities and Challenges

Vázquez-Domínguez, I., Garanto, A., & Collin, R. W. J. (2019) · Genes

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 80

High-Resolution Homozygosity Mapping Is a Powerful Tool to Detect Novel Mutations Causative of Autosomal Recessive RP in the Dutch Population

Collin, R. W. J., van den Born, L. I., Klevering, B. J., de Castro-Miró, M., Littink, K. W., Arimadyo, K., Azam, M., Yazar, V., Zonneveld, M. N., Paun, C. C., et al. (2011) · Investigative Opthalmology & Visual Science

Retinal Development and DisordersGenomics and Rare Diseases

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