| 1 | LTBP2, MSPKA |
| Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma - a distinct phenotype caused by recessive LTBP2 mutations. | |
| Khan AO, Aldahmesh MA, Alkuraya FS. | |
| Mol Vis 17:2570-9. Epub 2011 Oct 4. 2011 | |
| 2 | LTBP2, MSPKA |
| A homozygous mutation in LTBP2 causes isolated microspherophakia. (full Article Online) | |
| Kumar, A., Duvvari, M. R., Prabhakaran, V. C., Shetty, J. S., Murthy, G. J., Blanton, S. H. | |
| Hum. Genet. 439: 858-866. 2010 | |