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. Author manuscript; available in PMC: 2006 Feb 7.
Published in final edited form as: Arch Ophthalmol. 2003 Aug;121(8):1181–1183. doi: 10.1001/archopht.121.8.1181

graphic file with name nihms-7083-0001.jpg

Representative pedigrees showing the segregation of disease and the Met98Lys DNA sequence variant genotypes. M/M is homozygous for methionine at codon 98, while M/K is heterozygous for the methionine/lysine at codon 98. Square indicates male; circle, female; diagonal line, deceased; solid symbol, affected individual; and question mark, unknown allele.