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SAG mutations are responsible for the majority of cases of in the Japanese population and have an autosomal recessive pattern of inheritance. For a more thorough discussion of this subject the reader is referred to the LVII Edward Jackson Memorial lecture by Thaddeus P. Dryja, MD, entitled "Molecular of oguchi disease, fundus albipunctatus, and other forms of stationary due to compound heterozygosity including a novel deletion in the arrestin “is a rare autosomal recessive disease and known to be caused by mutations in the rhodopsin kinase (GRKl) or the Molecular of human color vision: the encoding blue, green, and red pigments. Molecular of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on cluomosome 1q. A homozygous 1-base pair deletion in the arrestin is a frequent cause of in Japanese. 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