A Clinical and Molecular Genetic Study of Autosomal-Dominant Stromal Corneal Dystrophy in British Population-Reference-Cited by-同舟云学术

A Clinical and Molecular Genetic Study of Autosomal-Dominant Stromal Corneal Dystrophy in British Population

Published:2005 Issue:6 Volume:37 Page:310-317
ISSN:0030-3747
Container-title:Ophthalmic Research
language:en
Short-container-title:Ophthalmic Res

Author:

EL-Ashry Mohamed Farouk,El-Aziz Mai Mohamed Abd,Hardcastle Alison J.,Bhattacharya Shomi S.,Ebenezer Neil D.

Publisher

S. Karger AG

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology,General Medicine

Reference27 articles.

1. Waring III GO, Mbekeani JN: Corneal dystrophies; in Leibowitz HW, Waring GO III (eds): Corneal Disorders: Clinical Diagnosis and Management, ed 2. Philadelphia, Saunders,1998, pp 245-251.

2. Assignment of Granular Corneal Dystrophy Groenouw Type I (CDGG1 ) to Chromosome 5q

3. Three autosomal dominant corneal dystrophies map to chromosome 5q

4. Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval.

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