PMC:1435744 / 4727-4982
Annnotations
craft-ca-core-ex-dev
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craft-ca-core-dev
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craft-sa-dev
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In addition, mutations of human CRX have been demonstrated to be associated with three types of photoreceptor diseases: autosomal dominant cone-rod dystrophy 2, autosomal dominant-type retinitis pigmentosa, and Leber's congenital amaurosis (LCA) [11-14]."}