Literature DB >> 1980096

X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq.

M Schwartz1, M Haim, D Skarsholm.   

Abstract

Linkage analysis in a family with X-linked myopia gave a positive LOD score (z = 4.8 at theta = 0) for linkage to F8C. These results suggest a provisional assignment for the locus of this syndrome to the distal part of the X chromosome at Xq28. Based on the clinical and genetic evidence, a redefinition of this clinical syndrome, named Bornholm Eye Disease (BED), was made to include amblyopia, myopia, and deuteranopia. Facultative signs were optic nerve hypoplasia, reduced electroretinographic flicker function, and non-specific retinal pigment abnormalities.

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Year:  1990        PMID: 1980096

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  56 in total

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2.  Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study.

Authors:  Christine Yi-Chin Chen; Katrina Jacqueline Scurrah; Jim Stankovich; Pam Garoufalis; Mohamed Dirani; Kelly Kathleen Pertile; Andrea Jane Richardson; Paul Mitchell; Paul Nigel Baird
Journal:  Hum Genet       Date:  2007-01-05       Impact factor: 4.132

3.  Dissecting the genetics of human high myopia: a molecular biologic approach.

Authors:  Terri L Young
Journal:  Trans Am Ophthalmol Soc       Date:  2004

4.  Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.

Authors:  Michelle McClements; Wayne I L Davies; Michel Michaelides; Terri Young; Maureen Neitz; Robert E MacLaren; Anthony T Moore; David M Hunt
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-02-15       Impact factor: 4.799

5.  A second locus for familial high myopia maps to chromosome 12q.

Authors:  T L Young; S M Ronan; A B Alvear; S C Wildenberg; W S Oetting; L D Atwood; D J Wilkin; R A King
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

6.  A single nucleotide polymorphism analysis of the LAMA1 gene in Japanese patients with high myopia.

Authors:  Sayaka Sasaki; Masao Ota; Akira Meguro; Ritsuko Nishizaki; Eiichi Okada; Jeewon Mok; Tetusya Kimura; Akira Oka; Yoshihiko Katsuyama; Shigeaki Ohno; Hidetoshi Inoko; Nobuhisa Mizuki
Journal:  Clin Ophthalmol       Date:  2007-09

7.  Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia.

Authors:  Zhikuan Yang; Xueshan Xiao; Shiqiang Li; Qingjiong Zhang
Journal:  Mol Vis       Date:  2009-02-09       Impact factor: 2.367

8.  The retinoic acid receptor alpha (RARA) gene is not associated with myopia, hypermetropia, and ocular biometric measures.

Authors:  S Veerappan; M Schäche; K K Pertile; F M A Islam; C Y Chen; P Mitchell; M Dirani; P N Baird
Journal:  Mol Vis       Date:  2009-07-17       Impact factor: 2.367

9.  AC and AG dinucleotide repeats in the PAX6 P1 promoter are associated with high myopia.

Authors:  Tsz Kin Ng; Ching Yan Lam; Dennis Shun Chiu Lam; Sylvia Wai Yee Chiang; Pancy Oi Sin Tam; Dan Yi Wang; Bao Jian Fan; Gary Hin-Fai Yam; Dorothy Shu Ping Fan; Chi Pui Pang
Journal:  Mol Vis       Date:  2009-11-05       Impact factor: 2.367

10.  Fine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36.

Authors:  Robert Wojciechowski; Joan E Bailey-Wilson; Dwight Stambolian
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