Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier11None of the authors has a financial interest relating to this article.-Reference-Cited by-同舟云学术

Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier11None of the authors has a financial interest relating to this article.

Published:2001-09 Issue:9 Volume:108 Page:1607-1620
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Craig Jamie E,Baird Paul N,Healey Danielle L,McNaught Andrew I,McCartney Paul J,Rait Julian L,Dickinson Joanne L,Roe Lynne,Fingert John H,Stone Edwin M,Mackey David A

Publisher

Elsevier BV

Subject

Ophthalmology

Reference22 articles.

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2. Genetic linkage of familial open angle glaucoma to chromosome 1q21–q31;Sheffield;Nat Genet,1993

3. Identification of a gene that causes primary open angle glaucoma;Stone;Science,1997

4. A novel myosin-like protein (Myocilin) expressed in the connecting cilium of the photoreceptor;Kubota;Genomics,1997

5. Analysis of Myocilin mutations in 1703 glaucoma patients from five different populations;Fingert;Hum Mol Genet,1999

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