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VSX2 in microphthalmia: a novel splice site mutation producing a severe microphthalmia phenotype

https://doi.org/10.1136/bjo.2009.159996

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    Footnotes

    • Funding Wellcome Trust.

    • Competing interests None declared.

    • Patient consent Informed consent for publication was granted by the family.

    • Provenance and peer review Not commissioned; externally peer reviewed.