Optic Atrophy, Cataract, and Neurologic Disorder
General: Autosomal dominant; similar to syndromes o 515g67f f Behr, Marinesco, Sjgren, and Friedreich, which are autosomal recessive.
Ocular: Cataract; optic atrophy.
Clinical: Neurologic disorder.
McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998.
Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007. World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/.
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