PMC:1435744 / 4727-4982 JSONTXT

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    craft-ca-core-ex-dev

    {"project":"craft-ca-core-ex-dev","denotations":[{"id":"T3477","span":{"begin":14,"end":23},"obj":"SO_EXT:sequence_alteration_entity_or_process"},{"id":"T3478","span":{"begin":27,"end":32},"obj":"NCBITaxon:9606"},{"id":"T3479","span":{"begin":33,"end":36},"obj":"PR_EXT:000005904"},{"id":"T3480","span":{"begin":97,"end":110},"obj":"CL:0000210"},{"id":"T3481","span":{"begin":121,"end":130},"obj":"GO:0030849"},{"id":"T3482","span":{"begin":140,"end":144},"obj":"CL:0000573"},{"id":"T3483","span":{"begin":145,"end":148},"obj":"CL:0000604"},{"id":"T3484","span":{"begin":162,"end":171},"obj":"GO:0030849"}],"text":" 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]."}

    craft-ca-core-dev

    {"project":"craft-ca-core-dev","denotations":[{"id":"T3283","span":{"begin":27,"end":32},"obj":"NCBITaxon:9606"},{"id":"T3284","span":{"begin":33,"end":36},"obj":"PR:000005904"},{"id":"T3285","span":{"begin":97,"end":110},"obj":"CL:0000210"},{"id":"T3286","span":{"begin":121,"end":130},"obj":"GO:0030849"},{"id":"T3287","span":{"begin":140,"end":144},"obj":"CL:0000573"},{"id":"T3288","span":{"begin":145,"end":148},"obj":"CL:0000604"},{"id":"T3289","span":{"begin":162,"end":171},"obj":"GO:0030849"}],"text":" 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]."}

    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]."}