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17. Two different alleles for deuteranomaly within a family with Leber's optic atrophy. Grützner P; Schrapp A Mod Probl Ophthalmol; 1974; 13(0):258-61. PubMed ID: 4548141 [No Abstract] [Full Text] [Related]
18. Hereditary optic atrophy. An autosomal dominant with incomplete penetrance. Shapiro LR; Raab EL; Leopold IH; Hirschhorn K Arch Ophthalmol; 1969 Mar; 81(3):359-62. PubMed ID: 5774293 [No Abstract] [Full Text] [Related]
19. Complete mitochondrial DNA sequence analysis in a family with early-onset dystonia and optic atrophy. Brown MD; Hosseini S; Steiner I; Wallace DC; Korn-Lubetzki I Mov Disord; 2004 Feb; 19(2):235-7. PubMed ID: 14978686 [TBL] [Abstract][Full Text] [Related]