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Korkko, J., Ritvaniemi, P., Haataja, L., Kaariainen, H., Kivirikko, K. I., Prockop, D. J., & Ala-Kokko, L. (1993). Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha-I-67 and that causes cataracts and retinal detachment: Evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy). The American Journal of Human Genetics, 53, 55-61.

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