Posterior chorioretinal atrophy and vitreous phenotype in a family with Stickler syndrome from a mutation in the COL2A1 gene
| Autor: | Vu, Cuong D, Brown, Jeremiah, Jr., Körkkö, Jarmo, Ritter, Robert, III, Edwards, Albert O |
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| Zdroj: | In Ophthalmology 2003 110(1):70-77 |
| Databáze: | ScienceDirect |
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