Article citationsMore>>

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.

has been cited by the following article:

Follow SCIRP
Twitter Facebook Linkedin Weibo
Contact us
Free SCIRP Newsletters
Copyright © 2006-2021 Scientific Research Publishing Inc. All Rights Reserved.