Körkkö, J., Ritvaniemi, P., Haataja, L., Kääriäinen, H., Kivirikko, K. I., Prockop, D. J., & Ala-Kokko, L. (1993). Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: Evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy).
Citação norma ChicagoKörkkö, J., P. Ritvaniemi, L. Haataja, H. Kääriäinen, K I. Kivirikko, D J. Prockop, and L. Ala-Kokko. Mutation in Type II Procollagen (COL2A1) That Substitutes Aspartate for Glycine Alpha 1-67 and That Causes Cataracts and Retinal Detachment: Evidence for Molecular Heterogeneity in the Wagner Syndrome and the Stickler Syndrome (arthro-ophthalmopathy). 1993.
MLA citiranjeKörkkö, J., et al. Mutation in Type II Procollagen (COL2A1) That Substitutes Aspartate for Glycine Alpha 1-67 and That Causes Cataracts and Retinal Detachment: Evidence for Molecular Heterogeneity in the Wagner Syndrome and the Stickler Syndrome (arthro-ophthalmopathy). 1993.