Functional study of SCCD pathogenic gene UBIAD1
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DOI: 10.3892/mmr.2021.12345
Abstract: Schnyder's crystalline corneal dystrophy (SCCD) is a rare autosomal dominant genetic disorder that is characterized by progressive corneal opacity, owing to aberrant accumulation of cholesterol and phospholipids in the cornea. A number of SCCD affected… read more here.
Keywords: study sccd; sccd pathogenic; functional study; gene ubiad1 ... See more keywords