Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy
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DOI: 10.1080/13816810.2019.1622023
Abstract: ABSTRACT Purpose: Cone-rod dystrophy (CRD) is an inherited retinal dystrophy that is transmitted via different modes of inheritance. Mutations in more than 30 genes have been identified to cause the disease. We aimed to investigate… read more here.
Keywords: dystrophy; rod dystrophy; form; crx gene ... See more keywords