A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract

Ítems similars

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• Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families
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• Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract
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• A novel GJA3 mutation causing autosomal dominant congenital perinuclear cataracts
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• Another evidence for a D47N mutation in GJA8 associated with autosomal dominant congenital cataract
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