VSX2 in microphthalmia: a novel splice site mutation producing a severe microphthalmia phenotype.
Saved in:
| Title: | VSX2 in microphthalmia: a novel splice site mutation producing a severe microphthalmia phenotype. |
|---|---|
| Authors: | Burkitt Wright EM, Perveen R, Bowers N, Ramsden S, McCann E, O'Driscoll M, Lloyd IC, Clayton-Smith J, Black GC |
| Source: | The British journal of ophthalmology [Br J Ophthalmol] 2010 Mar; Vol. 94 (3), pp. 386-8. |
| Publication Type: | Case Reports; Letter; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: BMJ Pub. Group Country of Publication: England NLM ID: 0421041 Publication Model: Print Cited Medium: Internet ISSN: 1468-2079 (Electronic) Linking ISSN: 00071161 NLM ISO Abbreviation: Br J Ophthalmol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
Be the first to leave a comment!
