Ocular Histopathologic Characteristics of Cobalamin C Type Vitamin B12 Defect With Methylmalonic Aciduria and Homocystinuria
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference11 articles.
1. Inherited disorders of cobalamin transport and metabolism;Fenton,1989
2. Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence. A treatable cause of dementia and myelopathy;Shinnar;N. Engl. J. Med.,1984
3. Epileptiform ocular movements with methylmalonic aciduria and homocystinuria;Cogan;Am. J. Ophthalmol.,1980
4. Retinal degeneration in vitamin B12 disorder associated with methylmalonic aciduria and sulfur amino acid abnormalities;Robb;Am. J. Ophthalmol.,1984
5. Clinical heterogeneity in cobalamin C variant of combined methylmalonic aciduria and homocystinuria;Mitchell;J. Pediatr.,1986
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