Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene-Reference-Cited by-同舟云学术

Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene

Published:2000-10 Issue:2 Volume:26 Page:237-241
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Akama Tomoya O.,Nishida Kohji,Nakayama Jun,Watanabe Hitoshi,Ozaki Kouichi,Nakamura Takahiro,Dota Atsuyoshi,Kawasaki Satoshi,Inoue Yoshitsugu,Maeda Naoyuki,Yamamoto Shuji,Fujiwara Tsutomu,Thonar Eugene J.-M.A.,Shimomura Yoshikazu,Kinoshita Shigeru,Tanigami Akira,Fukuda Michiko N.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1000_237.pdf

Reference25 articles.

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2. Edward, D.P. et al. Heterogeneity in macular corneal dystrophy. Arch. Ophthalmol. 106, 1579–1583 (1988).

3. Vance, J.M. et al. Linkage of a gene for macular corneal dystrophy to chromosome 16. Am. J. Hum. Genet. 58, 757–762 (1996).

4. Jonasson, F. et al. Macular corneal dystrophy in Iceland. A clinical, genealogic, and immunohistochemical study of 28 patients. Ophthalmology 103, 1111–1117 (1996).

5. Liu, N.P. et al. Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I gene. Am. J. Hum. Genet. 63, 912–917 (1998).

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