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2. Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p

Author

Tsujikawa, Motokazu, Kurahashi, Hiroki, Tanaka, Toshihiro, Okada, Masaki, Yamamoto, Syuji, Maeda, Naoyuki, Watanabe, Hitoshi, Inoue, Yoshitsugu, Kiridoshi, Akira, Matsumoto, Kouki, Ohashi, Yuichi, Kinoshita, Shigeru, Shimomura, Yoshikazu, Nakamura, Yusuke, and Tano, Yasuo

Subjects
Corneal diseases -- Causes of, Eye diseases -- Research, Genetic disorders -- Research, Biological sciences
Abstract

Research has determined a genetic locus for the autosomal recessive disorder gelatinous drop-like corneal dystrophy (GDLD), which causes amyloid deposits that impair vision. After linkage analyses were performed on affected Japanese subjects, homozygosity mapping placed the disease locus on the chromosome 1 short arm. Increased accuracy was obtained through haplotype analysis.

Published
1998

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