Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern Greece
Author(s) -
George Kitsos,
Zacharias Petrou,
Maria Grigoriadou,
John R. Samples,
Alex W. Hewitt,
Haris Kokotas,
Aglaia GiannouliaKarantana,
David A. Mackey,
Mary K. Wirtz,
Marilita Moschou,
John P.A. Ioannidis,
Michael B. Petersen
Publication year - 2010
Publication title -
clinical ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 56
eISSN - 1177-5483
pISSN - 1177-5467
DOI - 10.2147/opth.s8974
Subject(s) - mutation , myocilin , genotyping , medicine , founder effect , genetics , population , open angle glaucoma , glaucoma , ophthalmology , gene , genotype , haplotype , biology , environmental health
Mutations in the MYOC gene have been shown to explain 5% of unrelated primary open angle glaucoma (POAG) in different populations. In particular, the T377M MYOC mutation has arisen at least three separate times in history, in Great Britain, India, and Greece. The purpose of this study is to investigate the distribution of the mutation among different population groups in the northwestern region of Greece.
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