Optic Atrophy-Spastic Paraplegia Syndrome
General: Degenerative disorder of CNS 737b19h associated with optic atrophy; sex-linked.
Ocular: Optic atrophy.
Clinical: Neurologic spastic paraplegia,
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/.
Went LN. A sex-linked heredodegenerative neurological disorder associated with Leber's optic atrophy. Genetic aspects. Acta Genet Stat Med 1964; 14:220-239.
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