To investigate whether mutations in NPHP5 can cause Leber congenital amaurosis (LCA) without early-onset renal disease. DNA samples from 276 individuals with non-syndromic LCA were screened for variations in the NPHP5 gene.
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However, over the last 30 to 40 years, there has been a large volume of literature which has been published and presents itself as foundational work to both the Creighton Model FertilityCare System and the women’s health science of…