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<http://identifiers.org/pubmed/21907015> <http://purl.org/dc/terms/title> "Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma." <http://purl.org/np/RAr22T6UfXMZdb4imFEWOlE0QUylX_p8OtjURXU8-peRU#provenance> .
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