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I. Schrauwen, M. Sommen, C. Claes, J. Pinner, M. Flaherty, F. Collins and G. Van Camp Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome Clinical Genetics 86

Version of Record online: 23 SEP 2013 | DOI: 10.1111/cge.12265

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