Founder Effect for Thr377Met Myocilin Mutation in 8 POAG Families From Differing Ethnic Backgrounds
Mary K. Wirtz(Legacy Health), Subbiah R. Krishnadas, David A. Mackey(Lions Eye Institute), Janey L. Wiggs(Broad Institute), R. Rand Allingham(Duke Medical Center), M.B. Petersen(Institute of Child Health), Periasamy Sundaresan(Aravind Eye Hospital), J. R. Samples(Oregon Health & Science University), Irma Järvelä(University of Helsinki)
Investigative Ophthalmology & Visual Science
May 1, 2006
Cited by 0
Related Papers
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
|Nature Genetics|2015|1.6k
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
|PLoS Genetics|2012|443
Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
|Nature Genetics|2018|384
Consensus recommendations for trabecular meshwork cell isolation, characterization and culture
|Experimental Eye Research|2018|345
In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome: Figure 1
|Journal of Medical Genetics|2003|281