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Korkko J., Ritvaniemi P., Haataja L., Kaariainen H., Kivirikko K.I., Prockop D.J., Ala-Kokko L. 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). - Am.J.Hum.Genet., 1993, v. 53, p. 55-61.

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