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See Latest ArticlesA case of oculodentodigital dysplasia syndrome with novel GJA1 gene mutation
Japanese Journal of Ophthalmology, 11/10/09
Himi M et al. – A novel GJA1 mutation was detected in a Japanese ODDD patient. Glaucoma complications associated with ODDD have already been reported. Careful long–term monitoring and treatment are also necessary.
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